Krishna sarmapathy

doi:10.19080/OMCIJ.2019.08.555739

Research Article

NNRTI (Non-Nucleoside Reverse Transcriptase Inhibitor) Drug AZT and Their Preparation & Determination A Patent Evaluation of Efavirenz

Krishna sarmapathy*

Department of Organic Chemistry, Head IPL research Centre, India

Submission: April 04, 2019; Published: May 20, 2019

*Corresponding author: Krishna Sarmapathy, Department of Organic Chemistry, Head IPL research Centre, India

How to cite this article: Krishna sarmapathy. NNRTI (Non-Nucleoside Reverse Transcriptase Inhibitor) Drug AZT and Their Preparation & Determination A Patent Evaluation of Efavirenz. Organic & Medicinal Chem IJ. 2019; 8(3): 555739. DOI: 10.19080/OMCIJ.2019.08.555739

Abstract

Human immunodeficiency virus type-1 (HIV-1) is the causative agent for the transmission and development of the acquired immunodeficiency syndrome (AIDS).Efavirenz (II) a potent NNRTI, is a significant component of a very effective (protease sparing) regimen when co administered with AZT and 3TC [1]. Importance of Efavirenz led to the development of several strategies for its synthesis, and preparation was described in this paper, the world great potential drug Efavirenz still inaccessible to millions of people because of its atom economy and toxic [2]. Patent evaluation on process patents and well defined summary of patents . During the course of drug development most of the world pharmaceutical companies attempt well in the handling of environment friendly Efavirenz development especially Merck. We have surprisingly found that compound of Efavirenz can be prepared in good yield and high purity by Cyclisation of compound of (S)-2-(2-amino-5-chlorophenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn-2-ol with urea. Finally, Analytical method for determination Efavirenz has the absorbance maxima at 561 nm for the first order derivative visible-Spectrophotometric method

Keywords: HIV-1 AIDS AZT DTG Benz oxazinones Efavirenz; Urea Cyclisation crystallization UV spectrophotometric method ART CPA

Efavirenz, DMP 266

Efavirenz, L-743725((+)-enantiomer), DMP-266, L-741211(racemate), L-743726, Stocrin, Sustiva (S)-(-)-6-Chloro-4-(cyclopropylethynyl)-4-(trifluoromethyl)-2,4-dihydro-1H-3,1-benzoxazin-2-one. Now India recommends efavirenz (EFV)‐ based antiretroviral treatment (ART) to treat HIV, which is currently cheaper than DTG-based ART. However, as pharmaceutical licenses on DTG are now lifting in India, generic versions of DTG are likely to bring its cost close to that of EFV. Research from the USA and Europe, where DTG is recommended as the first option for treatment, suggests DTG has more tolerable side effects, can enable people to suppress HIV levels quickly and is less likely to lead to drug resistance [3].

As a result, DTG’s use in these countries has substantially reduced the number of people who fail first‐line treatment and are lost to care or require a switch to second‐line ART. Using a mathematical simulation model of how HIV can advance and how it responds to treatment, the study, published by the Journal of International AIDS Society, examined the clinical and economic impact DTG could have on India’s HIV response in comparison to EFV. Researchers found using DTG as the first option for HIV treatment would be cost‐effective, and potentially cost‐saving, for India’s public health system. At 48 weeks, modellingsuggests90% of people on DTG would be virally suppressed compared to 82% of those on EFV. Longer term, DTG was projected to increase the proportion of people living with HIV on treatment who were still alive after five years from 76.7% to 83%.Crucially, researchers found DTG had the potential to avert 13,000 new HIV infections over five years, equivalent to a 20% decrease in HIV incidence, resulting in a saving of US$800,000 in projected care costs. When all factors are taken into account, care costs for the number of people initiating treatment on EFV were estimated to be US$139 million at two years and US$590 million at five years. In comparison, the care costs for DTG at two years was found to be lower at US$137 million and cost-neutral at five years at US$590 million. Cost increases linked to DTG were identified by the model, although these reflect the fact that more people are likely to live longer when on DTG, incurring greater lifetime care costs [4].

As a result, the authors recommend that when generic DTG becomes available in India, if priced at no more than $180 per person per year, it would be cost-effective for India to switch to DTG as first‐line treatment.

The research is particularly timely as India changed its treatment guidelines in 2017 to recommend that people living with HIV start treatment as soon as possible, regardless of theirCD4 count. As a result, the cost of ART is becoming an increasingly central consideration to ensure treatment can be provided to all those now eligible.

Merck Synthesis of Efavirenz- History

Efavirenz was approved by the FDA on September 21, 1998, making it the 14th approved antiretroviral drug. Efavirenz is a non-nucleoside reverse transcriptase inhibitor being studied clinically for use in the treatment of HIV infections and AIDS. Efavirenz chemically known as (-) 6-Chloro-4-cyclopropylethynyl- 4-trifluoromethyl- 1, 4- dihydro-2H-3, 1-benzoxa zin-2-one, is a highly potent non-nucleoside reverse transcriptase inhibitor (NNRTI).A number of compounds are effective in the treatment of the human immunodeficiency virus (HIV) which is the retrovirus that causes progressive destruction of the human immune system. Effective treatment through inhibition of HIV reverse transcriptase is known for non- nucleoside-based inhibitors. Benz oxazinones have been found to be useful non-nucleosidebased inhibitors of HIV reverse transcriptase.(-) β-chloro^- cyclopropylethyny M-trifluoromethyl-l ,4-dihydro-2H-3,l -ben zoxazin-2-one (Efavirenz) is efficacious against HIV reverse transcriptase resistance [5]. Due to the importance of (-)6-chloro- 4-cyclopropylethynyl-4-trifluoromethyl-l,4-dihydro-2H-3,l-ben zoxazin-2- one, economical and efficient synthetic processes for its production needs to be developed. The product patent US5519021. discloses the preparation of Efavirenz, in Example-6, column-29, involving cyclisation of racemic mixture of 2-(2-amino- 5-chlorophenyl)-4- cyclopropyl-l,l,l-trifluoro-3-butyn-2-ol using l, l ‘-carbonyl diimidazole as carbonyl delivering agent to give racemic Efavirenz. Further, resolution of the racemic Efavirenz is carried out using (-) camphanic acid chloride to yield optically pure Efavirenz. However, research article published in the Drugs of the future, 1998, 23(2), 133-141 discloses process for manufacture of optically pure Efavirenz. The process involves cyclisation of racemic 2-(2-amino-5-chlorophenyl)-4-cyclopropyl-l, 1, l-trifluoro-3-butyn-2- ol using 1, 1-carbonyldiimidazole as carbonyl delivering agent to give racemic Efavirenz and further resolution by (-) camphanic acid chloride [6]. Similarly, research article published in Synthesis 2000, No. 4, 479-495 discloses stereo selective synthesis of Efavirenz (95%yield, 99.5%ee), as shown below (Figure 1)

Organic and Medicinal Chemistry International Journal

Even though many prior art processes report method for the preparation of Efavirenz, each process has some limitationswith respect to yield, purity, plant feasibility etc. Hence in view of the commercial importance of Efavirenz there remains need for an improved process. US 6 028 237 discloses a process for the manufacture of optically pure Efavirenz. The synthesis of efavirenz and structurally similar reverse transcriptase inhibitors are disclosed in US Patents 5,519,021, 5,663,169, 5,665,720 and the corresponding PCT International Patent Application WO 95/20389, which published on August 3, 1995 [7].

Additionally, the asymmetric synthesis of an enantiomeric benzoxazine by a highly enantioselective acetylide addition and cyclization sequence has been described by Thompson, et al., Tetrahedron Letters 1995, 36, 8937-8940, as well as the PCT publication, WO 96/37457, which published on November 28, 1996.Additionally, several applications have been filed which disclose various aspects of the synthesis of(-)-6-chloro- 4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1- benzoxazin-2-one including: 1) a process for making the chiral alcohol, U.S.S.N. 60/035,462, filed 14 January 1997; 2) the chiral additive, U.S.S.N. 60/034,926, filed 10 January 1997; 3) thecyclization reaction, U.S.S.N. 60/037,059, filed 12 February 1997; and the anti-solvent crystallization procedure, U.S.S.N. 60/037,385 filed 5 February 1997 and .S.S.N. 60/042,807 filed 8 April 1997 (Figures 2 & 3) [8].

Efavirenz has been obtained by two related ways: 1) The acylation of 4-chloroaniline (I) with pivaloyl chloride (II) by means of Na2CO3 in toluene gives the expected anilide (III), which is acylated with ethyl trifluoroacetate by means of butyllithium in THF yielding, after hydrolysis with HCl, 2′-amino- 5′-chloro-2,2,2-trifluoroacetophenone (IV). The benzylation of (IV) with 4-methoxybenzyl chloride (V) in basic alumina affords the protected acetophenone (VI), which is regioselectively condensed with cyclopropylacetylene (VII) [obtained by cyclization of 5-chloro-1-pentyne (VIII) by means of butyllithium in cyclohexane] by means of butyllithium in THF in the presence of (1R,2S)-1-phenyl-2-(1-pyrrolidinyl)-1-propanol (IX) giving the (S)-isomer of the tertiary alcohol (X) exclusively. The cyclization of (X) with phosgene and triethylamine or K2CO3 in toluene/ THF yields the benzoxazinone (XI), which is finally deprotected with ceric ammonium nitrate in acetonitrile/water. 2) The condensation of 2′-amino-5′-chloro-2,2,2-trifluoroacetophenone (IV) with cyclopropylacetylene (VIII) by means of butyllithium or ethylmagnesium bromide in THF gives (?-2-(2-amino-5- chlorophenyl)-4-cyclopropyl-1,1,1-trifluoro-3-butyn-2-ol (XII). The cyclization of (XII) with carbonyldiimidazole (XIII) in hot THF yields the racemic benzoxazinone (XIV). Compound (XIV) is submitted to optical resolution by condensation with (S)-(- )-camphanoyl chloride by means of dimethyl aminopyridine (DMAP) in dichloromethane to give the acyl derivative (XVI) as a diastereomeric mixture that is resolved by crystallization and finally decomposed with HCl in ethanol or butanol [9].

Corley EG, Thompson AS, Huntington MF, Grabowski EJJ, use of an ephedrine alkoxide to mediate enantioselective addition of an acetylide to a prochiral ketone: Asymmetric synthesis of the reverse transcriptase inhibitor L-743,726 Tetrahedron Lett1995,36,(49):8937-40 [10].

EP 1332757 A1

When a commercial market already exists for the RMs used in synthesizing an API, their cost can be rather modest. When RMs used in synthesizing an API have no other commercial use, however, they can contribute very substantially to API cost. With a continued growth of volume demand, improved chemistry and competition from multiple suppliers, however, the cost of API RMs can greatly decrease over time. The inhibitor of HIV-1 RT, EFV, provides an illustration of this situation. Cyclopropylacetylene (CPA) is an RM for the synthesis of EFV (Figure 4). During clinical trials, when the demand for CPA was only a few metric tons, this material was produced at a price of USD800-1,350/kg. When the drug was first approved in 1998, and demand for CPA was about 50 metric tons per year, the price of CPA had fallen to USD350/kg. Today, with global demand for EFV at greater than 1,000 metric tons/year, CPA can be purchased for about USD50-60/kg. In the earliest stages of production, nearly 1 kg of CPA was needed toproduce a kilogram of EFV. Current production processes are more efficient; roughly 3 kg of EFV is now produced for each 1 kg of CPA used. From this it can be roughly estimated that the contribution of CPA to the cost of EFV API production has fallen from as high as USD425/kg to about USD17-20/kg today [11].

The most recent chemistry for asymmetric alkylation of manufacturing EFV uses inexpensive, safe reagents and processing at ambient temperature to reach EFV pricing that would have been thought impossible when the drug was launched by Dupont Pharmaceuticals in 1998Biao J, Yugui S. inventors; Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, assignee. Amino alcohol ligand and its use in preparation of chiral propargylic tertiary alcohols and tertiary amines via enantioselective addition reaction. US Patent 7,439,400. 2008 October 21 [12].

Bollu RB, Ketavarapu NR, Indukuri VSK, Gorantla SR, Chava S. inventors; Laurus Labs Private Limited, assignee. Efficient process to induce enantioselectivity in procarbonyl compounds. US PatentApplication 2012/0264933 A1. 2012 October 18.FPPs for adult ART are usually capsules or tablets. A general rule-of-thumb is that an FPP as a conventional, solid oral dosage formulation costs about 33-40% more than the corresponding API in a competitive market (Figure 4a). It has been widely quoted, conversely, that APIs contribute about 60-80% of the cost of an FPP. The API contribution to FPP cost increases with the complexity of synthesis and API cost per kilogram. Although marketing is a substantial incremental cost for originator pharmaceutical companies, generic producers do not incur high marketing costs for ART [13].

To a solution of trifluoroethanol and (IR, 2S)-N-pyrrolidinyl norephedrine in THF (9L) under nitrogen is added a solution of diethylzinc in hexane at 0°C slowly enough to keep the temperature below 30°C. The mixture is stirred at room temperature for 0.5~1h. In another dry flask a solution of chloromagnesium cyclopropyl acetylide is prepared as follows: To neat cyclopropyl acetylene at 0°C is added a solution of rc-butylmagnesium chloride slowly enough to keep the internal temperature < 30°C. The solution is stirred at 0°C for ~40 min and transferred to the zinc reagent via cannula with 0.36 L of THF as a wash. The mixture is cooled to -10°C and ketoaniline la is added. The mixture is stirred at -2 to -8°C for 35 h, warmed to room temperature, stirred for 3 h, and quenched with 30% potassium carbonate over 1.5 h. The mixture is stirred for 4h and the solid is removed by filtration and washed with THF (2 cake volume). The wet solid still contains -18 wt% of pyrrolidinyl norephedrine and is saved for further study. The filtrate and wash are combined and treated with 30% citric acid. The two layers are separated. The organic layer is washed with water (1.5 L). The combined aqueous layers are extracted with 2.5 L of toluene and saved for norephedrine recovery. The toluene extract is combined with the organic solution and is concentrated to ~ 2.5L. Toluene is continuously feeded and distilled till THF is not detectable by GC. The final volume is controlled at 3.9 L. Heptane (5.2 L) is added over 1 h. The slurry is cooled to 0°C, aged for 1 h, and filtered. The solid is washed with heptane (2 cake volume) and dried to give 1.234 Kg (95.2% yield) of amino alcohol 3 as a white crystalline. The material is 99.8 A% pure and 99.3% ee [14].

To a three necked round bottom flask, equipped with a mechanical stirrer, nitrogen line, and thermocouple, was charged the solid amino alcohol 3, MTBE (500 L), and aqueous KHCO3 (45 g in 654 mL H2O). Solid 4-nitrophenyl chloroformate was added, in 4 batches, at 25°C. During the addition the solution pH was monitored. The pH was maintained between 8.5 and 4 during the reaction and ended up at 8.0. The mixture was stirred at 20-25°Cfor two hours. Aqueous KOH (2N) was added over 20 minutes, until the pH of the aqueous layer reached 11.0.

The layers were separated, and 500 mL brine was added to the MTBE layer. 0.1 N Acetic acid was added until the pH was 6-7. The layers were separated, and the organic phase was washed with brine (500 mL). At this point the mixture was solvent switched to EtOH/IPA and crystallized as recited in Examples 5 and 6. To a three necked round bottom flask, equipped with a mechanical stirrer, nitrogen line, and thermocouple, was charged the solid amino alcohol 3a, toluene (500mL), and aqueous KHCO3 (86.5g in 500L H2O). Phosgene solution in toulene was added at 25°C, and the mixture was stirred at 20-25°C for two hours.The layers were separated, and the organic phase was washed with brine (500 mL). At this point the mixture was solvent switched to EtOH/IPA and crystallized as recited in Examples 5 and 6.

To a three necked round bottom flask, equipped with a mechanical stirrer, nitrogen line, and thermocouple, was charged the solid amino alcohol 3a, MTBE (500 mL), and aqueous KHCO3 (86.5 g in 500mL H2O). Phosgene gas was slowly passed into the solution at 25°C, until the reaction was complete. The layers were separated, and the organic phase was washed with brine (500mL). At this point the mixture was solvent switched to EtOH/IPA and crystallized as recited in Examples 5 and 6.

Crystallization of efavirenz from 30% 2-Propanol in Water using a ratio of 15 ml solvent per gram efavirenz Using Controlled Anti-Solvent Addition on a 400g Scale. 400 g. of efavirenz starting material is dissolved in 1.8L of 2- propanol. The solution is filtered to remove extraneous matter. 1.95 L of deionized (DI) water is added to the solution over 30 to 60minutes. 10 g. to 20g. of efavirenz seed (Form II wetcake) is added to the solution. The seed bed is aged for 1 hour. The use of Intermig agitators is preferred to mix the slurry. If required (by the presence of extremely long crystals or a thick slurry), the slurry is wet milled for 15-60 seconds. 2.25 L of DI water is added to the slurry over 4 to 6 hours. If required (by the presence of extremely long crystals or a thick slurry), the slurry is wet- milled for 15-60 seconds during the addition. The slurry is aged for 2 to 16 hours until the product concentration in the supernatant remains constant. The slurry is filtered to isolate a crystalline wet cake. The wet cake is washed with 1 to 2 bed volumes of 30 % 2-propanol in water and then twice with 1 bed volume of DI water each. The washed wet cake is dried under vacuum at 50°C [15].

Crystallization of efavirenz from 30% 2-Propanol in Water using a ratio of 15 ml solvent per gram efavirenz Using a Semi- Continuous Process on a 400 g Scale. 400 g. of efavirenz starting material is dissolved in 1.8 L of 2- propanol. A heel slurry is produced by mixing 20 g. of Form II efavirenz in 0.3 L of 30 % (v/v) 2-propanol in water or retaining part of a slurry from a previous crystallization in the crystallizer. The dissolved batch and 4.2L of DI water are simultaneously charged to the heel slurry at constant rates over 6 hours to maintain a constant solvent composition inthe crystallizer. Use of Intermit agitators during the crystallization is preferred. During this addition the slurry is wet milled when the crystal lengths become excessively long, or the slurry becomes too thick. The slurry is aged for 2 to 16 hours until the product concentration in the supernatant remains constant. The slurry is filtered to isolate a crystalline wet cake. The wet cake is washed with 1 to 2 bed volumes of 30% 2-propanol in water and then twice with 1 bed volume of DI water each. The washed wet cake is dried under vacuum at 50°C [16] Example 7.

A solution of diethyl zinc in hexane was added to a solution of trifluoroethanol (429.5 g, 4.29’mol) and (IR, 2S)-N-pyrrolidinyl norephedrine (1.35kg, 6.58mol) in THF (9 L), under nitrogen, at 0°C. The resulting mixture was stirred at room temperature for approx. 30 min. In another dry flask a solution of chloromagnesiumcyclopropylacetylide was prepared as follows. To a solution of n- butyl magnesium chloride in THF (2M, 2.68L, 5.37mol) was added neat cyclopropyl acetylene at 0°C keeping the temperature <25°C. The solution was stirred at 0°C for 1~2 h. The solution of chloromagnesium cyclopropylacetylide was then warmed to room temperature and was transferred into the zinc reagent via cannula over 5 min followed by vessel rinse with 0.36 L of THF. The resulting mixture was aged at ~30°C for 0.5 h and was then cooled to 20°C. The ketoaniline 1 (1.00kg, 4.47 mol) was added in one portion as a solid, and the resulting mixture was stirred at 20- 28°C for 3h. The reaction was quenched with 30% aq. potassium carbonate (1.2L) and aged for 1 h. The solid waste was filtered and the cake was washed with THF (3 cake volumes). The filtrate and wash were combined, and solvent switched to IP Ac [17].

The IPAc solution of product 3 and pyrrolidinyl norephedrine was washed with citric acid (3.5L) and with water (1.5L). The combined aqueous layers were extracted with IPAc (2L) and saved for norephedrine recovery. To the combined organic layers was added 12N HC1 (405mL, 4.88mol), to form a thin slurry of the amino alcohol-HC1 salt. The mixture was aged for 30 min at 25°C and was then dried azeotropically. The slurry was aged at 25°C for 30 min and filtered. The cake was washed with 2.5 L of IPAc and dried at 25°C under vacuum/nitrogen for 24 h to give 1.76 kg of the wet HC1 salt. The salt was dissolved in a mixture of MTBE (6L) and aq Na2CO3 (1.18 kg in 6.25 L water). The layers were separated, and the organic layer was washed with 1.25 L of water. The organic layer was then solvent switched into toluene. Heptane (5 L) was added over 1h at 25°C. The slurry was cooled to 0°C, aged for 1h, and filtered. The solid was washed with heptane (2 cake volumes) and was dried to give 1.166kg (90% overall yield) of amino alcohol 3 as a white crystalline solid figure 4(b).

Norephedrine Recovery

The aqueous solution was basified to pH13 using 50% as NaOH and extracted with heptane (2L). The heptane solution was washed with water (1L) and concentrated to remove residual IPAc and water. The final volume was adjusted to about 3 L. The heptane solution was cooled to -20°C, aged for 2h, and filtered. The solid was washed with cold heptane (1 cake volume) and dried to give 1.269 kg solid (94% recovery).

Intermediate preparation: The key intermediate of efavirenz: (S)-l-(2-amino-5-chlorophenyl)-1-trifluoromethyl-3- cyclopropyl-2-propyne-1-ol (1) was prepared. P-Chloroaniline (2) reacted with pivaloyl chloride to give N-(4-chlorophenyl)- 2,2-dimethylpropanamide (4). After a Friedel-Crafts acylation of compound 4 catalyzed by aluminum trichloride, and a hydrolysis under acidic conditions, 4-chloro-2-(trifluoroacetyl)aniline hydrochloride (5) was obtained. In this step, the hazardous reagent n-butyllithium was abolished. Compound 5 was basified to afford 4-chloro-2-(trifluoroacetyl)aniline (6). Then compound 6 reacted with chloromagnesium cyclopropylacetylide under the catalytic system formed by zinc chloride and (1R,2S)-1-phenyl-2- (1-pyrrolidinyl)-1-propanol (7) and a small amount of purified 1 to obtain the target compound 1 by asymmetric autocatalysis with an overall yield of 69.5%(based on 2). In the last step, zinc chloride was used instead of diethylzinc, the yield was increased from 79% to 85.6%. And ligand 7 was recovered with a recovery rate of 98%, which could reduce the cost successfully. This improved synthetic route has mild reaction conditions and the yield of each step was excellent Figure 4(c).

Materials and Methods

General procedure- 1H NMR spectra were recorded on a Gemini 300MHz FT NMR spectrometer; the chemical shifts are reported in δ ppm relative to TMS. The IR spectra were recorded in the solid state as KBr dispersion using Perkin Elmer Spectrophotometer. The mass spectra were recorded on Shimadzu LCMS-QP8000, LC-MS and AB-4000 Q-trap LC-MS/MS Figure 4(d).

A solution of (S)-5-chloro-α-(cyclopropylethynyl)-2-amino- α-(trifluoroethyl)benzene methanol (I) (10 gm, 0.034mole) andurea (2.48 gm, 0.0414 mole in toluene are refluxed in the presence of para-tolunesulphonic acid (PTSA)(0.31 gm, 0.0006 mole) for 20 hrs. After completion of the reaction as monitored by Thin Layer Chromatorgraphy (TLC), the reaction mixture was cooled to room temperature and then 30 ml of water was added. The obtained aqueous layer was extracted with toluene. The combined toluene layers were concentrated under reduced pressure. The obtained residue was cooled to room temperature and 30 ml of methanol was added and stirred. Methanol was distilled of to remove the toluene traces. Again, methanol was added to the residue and cooled to 10-15ºC Figure 4(e).

To this residue water was added at 10-15ºC and stirred for 3 hrs. The obtained white solid was re-crystallized in toluene and heptane mixture to get 9.2gms of (4S)-6-chloro- 4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H- 3,1-benzoxazin-2-one (II) (Efavirenz). 1H NMR (300MHz in DMCO-d6): δ 0.782-0.815 (m, 2H), 0.908-0.956 (m,2H), 1.557- 1.646 (m, 1H, cyclopropyl), 6.98-7.013(d, 1H), 7.45(s, 1H), 7.55- 7.58 (dd, 1H), 11.11(s, 1H).

Mass

M/z; 314.2, in negative ion mode. Yield: 85%, MR: 136-139°C, SOR -92.8°(c 0.3 in MeOH) Chemicals and reagents Ethanol was used for the quantification of efavirenz which was procured from Sigma Aldrich. EFA film coated tablet of strength 600 mg Sustiva (Bristo-Myers Squibb-Germany) and Efavir (Cipla Ltd-India) were procured from the market. The pure sample of efavirenz for the research work was procured from Shasun Pharmaceuticals Ltd, Pondicherry. Hydrochloric acid, sodium hydroxide, and - naphthol were purchased from Sigma Aldrich. All the chemicals and reagents for the development of new analytical method to estimate efavirenz was of analytical grade. Preparation of - naphthol reagent Accurately 1g of - naphthol was weighed and transferred to 100ml volumetric flask. To it 30ml of 0.1N NaOH was added and shacked such that - naphthol gets completely dissolved in NaOH. Make up the volume to 100ml with 0.1N NaOH. Preparation of Efavirenz standard solutions 100mg of the drug was weighed and transferred in to 100ml volumetric flask, to it ethanol was added, and volume was made up to 100ml with ethanol. From this 10ml was transferred to 100ml volumetric flask and volume was made up to 100ml with ethanol such that the solution gives the concentration of 100/. Preparation of reagent blank. The reagent blank was prepared in the same manner as discussed, omitting the standard drug solution. Procedure for the analysis of tablet formulation Twenty tablets of Efavirenz (600mg) and Sustiva were purchased from local market. Accurately weighed and finelypowdered. The weight of the tablet equivalent to 100mg from each brand was accurately weighed and extracted with ethanol. The yellow colored complex (Scheme-1) having final concentration of 100mg/ml of each brand was prepared. The absorbance of the solutions was measured at 561nm using reagent blank Figure (5).

Result and Discussion

Selection of analytical wavelength: Appropriate dilutions were prepared for drug from the standard stock solution and the solutions were scanned in the wavelength range of 400 - 800nm. Absorption maxima were found to be 561nm which was selected as wavelength of analytical measurement for this method. Calibration curve Appropriate volume of aliquots from standard Efavirenz stock solution II were transferred to different volumetric flasks of 10 ml capacity. To all the volumetric flasks 1ml of 1% sodium nitrite, 1ml of HCl and finally ℎ was added. The volume was adjusted to the mark with ethanol to obtain concentrations of 10, 12, 14, 16, 18 and 20 /. Absorbance of each solution blank was measured at 561nm and the graph of absorbance against concentration was plotted and is shown in figure 1. The regression equation and correlation coefficient were determined. The method was validated according to International Conference on Harmonization guidelines for validation of analytical procedures [9,10,11]. Efavirenz has the absorbance maxima at 561 nm for the first order derivative visible-Spectrophotometric method. The optical characteristics such as Beer’s limits, Limit of detection and Limit of quantification etc., in each method were calculated andthe results were presented in Table 1 respectively. The regression characteristics like slope (b), intercept (a), and correlation coefficient (R2) using the method of least squares were calculated and presented in Table 1 respectively. The results showed that the methods have reasonable precise. The validation parameters like Precision and Accuracy results were presented in Tables 2 & 3 for Visible Spectrophotometric method. There was no interference of excipients in recovery study of the method. From results, the method found applicable for both bulk and pharmaceutical dosage for the estimation of Efavirenz. Recovery studies. The recovery studies were carried out at three different level i.e. 80,100 and 120%. It was performed by adding known amount of standard drug solutions of Efavirenz to preanalysed tablets solutions (Figure 6). The resulting solutions were then reanalyzed by proposed methods. The results of recovery studies are shown in Tables 4 & 5.

Conclusion

After patent evaluation finally concluded that efavirenz US granted patent John Doney, “Amorphous efavirenz and the production thereof.” U.S. Patent US20070026073, issued February 01, 2007 ,process patent WO1999061026 both patents selected for process for preparation of efavirenz. We have surprisingly found that compound of Efavirenz can be prepared in good yield and high purity by Cyclisation of compound of (S)-2-(2- amino-5-chlorophenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn- 2-ol with urea as shown in the above scheme. This cyclization of compound of (S)-2-(2-amino-5-chlorophenyl)-4-cyclopropyl-1, 1, 1-trifluorobut-3-yn-2-ol is affected in a suitable reaction media which includes aromatic hydrocarbons, aqueous alcohols, ketones . more preferably toluene. Optionally, the above Cyclisation is conducted in presence of an acid. The suitableacids may include mineral acids for example hydrochloric acid, sulfuric acids etc. organic acids like ptoluenesulphonicacid, acetic acid and trifluoro acetic acid etc. The cyclization is conveniently affected at elevated temperatures, most conveniently at reflux temperature of the reaction mixture. We have described a novel synthesis for theAfter patent evaluation finally concluded that efavirenz US granted patent John Doney, “Amorphous efavirenz and the production thereof.” U.S. Patent US20070026073, issued February 01, 2007 ,process patent WO1999061026 both patents selected for process for preparation of efavirenz. We have surprisingly found that compound of Efavirenz can be prepared in good yield and high purity by Cyclisation of compound of (S)-2-(2- amino-5-chlorophenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn- 2-ol with urea as shown in the above scheme. This cyclization of compound of (S)-2-(2-amino-5-chlorophenyl)-4-cyclopropyl-1, 1, 1-trifluorobut-3-yn-2-ol is affected in a suitable reaction media which includes aromatic hydrocarbons, aqueous alcohols, ketones . more preferably toluene. Optionally, the above Cyclisation is conducted in presence of an acid. The suitableacids may include mineral acids for example hydrochloric acid, sulfuric acids etc. organic acids like ptoluenesulphonicacid, acetic acid and trifluoro acetic acid etc. The cyclization is conveniently affected at elevated temperatures, most conveniently at reflux temperature of the reaction mixture. We have described a novel synthesis for the