The present invention relates to an improved process for the preparation of2-(3-fluoro-4-(methyi-carbamoyI)phenyi-amino)-2-methyI-propionic acid ethyl ester comprising, 2-fluoro-4-nitrobenzoic acid (HI) is reacted with methanol in presence of acid to produce methyl 2-fluoro-4-nitrobenzoate of formula (X); which is r...

The present invention provides a simple, environmental friendly process for the preparation of crystalline form of Linezolid. The present invention also provides pure crystalline form of Linezolid in good yield.

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The present invention relates to an improved process for preparing the diamine intermediate, ethyl 3-(3-amino-4-(methylamino)-N-(pyridin-2-yl)benzamido)propanoate, compound of formula (I), used in preparation of Dabigatran. The present invention relates to a simple, cost-effective pro cess for preparing compound of ...

The present invention is directed towards novel process for the preparation of Rivaroxaban. The process is cost effective and industrially viable.

The present invention provides a novel process for the preparation of tert-butyl 2-((2R, 4S)-4-formyl-l,5-dioxaspiro[5.5]undecan-2-yl)acetate of formula (I). The present invention further relates to a process for the preparation of Rosuvastatin calcium by using the formula (I)

ABSTRACT: The present invention relates to a novel processes for preparing Rosuvastatin Calcium.

ABSTRACT TITLE: "AN IMPROVED PROCESSES FOR PREPARING LINEZOLID" The present invention provides simple, environmental friendly improved process for the preparation of Linezolid. The present invention also provides an alternate improved process for preparing Linezolid with good yield.

ABSTRACT: The present invention provides simple, environmental friendly improved processes for the preparation of Linezolid. The present invention also provides an alternate improved process for preparing Linezolid in good yield.

ABSTRACT TITLE: “PROCESS FOR THE PREPARATION OF TEDIZOLID PHOSPHATE” The present invention relates to a process for the preparation of Tedizolid Phosphate. The present invention is also provides industrial applicable, commercially and eco-friendly viable process for the preparation of Tedizolid Phosphate. ...

The present invention relates to crystalline form of Ozenoxacin and its process for the preparation.

PROCESS FOR THE PREPARATION OF FEBUXOSTAT The present invention relates to an improved, commercially viable and industrially advantageous process for the preparation of Febuxostat.

ABSTRACT TITLE: “PROCESS FOR THE PREPARATION OF DIMETHINDENE MALEATE” The present invention relates to a process for the preparation of Dimethindene maleate formula (I) by employing a key intermediate of 2-(2-(dimethylamino) ethyl-2, 3-dihydroinden-1-one acid salt formula (IIIa). The present invention also relates...

The present invention relates to amorphous form of Ozenoxacin. The present invention is also relates to improved, commercially viable and industrially advantageous process for the preparation of Ozenoxacin.

The present invention relates to improved, commercially viable and industrially advantageous process for the preparation of crystalline form III of Linezolid.

The present invention relates to a process for the preparation of (±)-Ritalinic acid hydrochloride with cost effective and industrial applicable by employing a novel step.

The present invention relates to improved process for the preparation of (S)-Dapoxetine or an acid addition salt thereof and also provides an enantiomerically pure form of Dapoxetine hydrochloride

The present invention relates to a process for the preparation of Fenticonazole nitrate of Formula (I) with commercially viable and industrial applicable process.

The present invention relates to an improved process for the preparation of Phenyramidol hydrochloride of Formula (I) with commercially viable and industrial applicable process.

The present invention provides a novel process for the preparation of 1-benzofuran-6-carboxylic acid of formula (II) by employing novel compound of [2-formyl-5-(methoxycarbonyl) phenoxy] acetic acid of formula (VI).

The present invention provides a novel process for the preparation of methyl-1-benzofuran-6-carboxylate of formula (II).

The present invention relates to an improved process for the preparation of Eberconazole nitrate by using Carbonyldiimidazole. The present invention is also relates to simple and cost effective process for the preparation of Eberconazole nitrate.

The present invention relates to a process for the preparation of N-(5-Chloro-2-nitrophenyl) phenyl amine, compound of formula (I) with high purity and good yield, which is a key intermediate for the preparation of Clobazam.

ABSTRACT TITLE: “NOVEL PROCESS FOR THE PREPARATION OF (+)-CIBENZOLINE SUCCINATE”. The present invention relates to a crystalline form of (+)-Cibenzoline succinate. The present invention is also related to a process for the preparation of (+)-Cibenzoline succinate with chiral purity greater than 99.9%. The present...

ABSTRACT TITLE: “NOVEL PROCESS FOR THE PREPARATION OF (-)-CIBENZOLINE SUCCINATE”. The present invention relates to a crystalline form of (-)-Cibenzoline succinate. The present invention is also related to a process for the preparation of (-)-Cibenzoline succinate with chiral purity greater than 99.9%. The presen...

The present invention provides a process for the preparation sodium (s)-4-oxo-4, 6, 7, 8-tetrahydropyrrolo [1, 2-a] pyridine-6-carboxylate of formula (II). The present invention is also provides commercially, synthetically by industrially applicable method to ensure the availability with high purity. ...

ABSTRACT TITLE: CRYSTALLINE FORM OF RIFAXIMIN The present invention relates to a novel crystalline form of rifaximin and process for its preparation thereof.

ABSTRACT TITLE: PROCESS FOR THE PREPARATION OF LINEZOLID FORM III The present invention relates to improved, commercially viable and industrially applicable process for the preparation of crystalline form III of Linezolid.

The present invention provides a process for the preparation E-isomer of Luliconazole (I) with substantially free of Z-isomer and unwanted salts.

The present invention relates to the novel compound of Ubiquinol di-Tocopherol succinate ester (I). The present invention further provides an improved, commercially viable and industrially advantageous process for the preparation of Ubiquinol di-Tocopherol succinate ester (I).

Abstract Title: PROCESS FOR THE PREPARATION OF PURE 3-n-BUTYLPHTHALIDE The present invention relates to an improved, commercially viable and industrially advantageous process for the preparation of 3-n-Butylphthalide. The present invention further provides a process for the preparation of highly pure 3-n-But...

ABSTRACT Title: “NOVEL SYNTHESIS OF FAVIPIRAVIR AND ITS INTERMEDIATE” The present invention relates to a novel process for the preparation of Favipiravir intermediate. The present invention is also relates to an improved, commercially viable and industrially advantageous process for the preparation of highly p...

ABSTRACT TITLE: “PURIFICATION PROCESS OF FAVIPIRAVIR” The present invention relates to purification process of Favipiravir. The present invention further relates to an improved, commercially viable, industrially advantageous, and environmental friendly process for the preparation of Favipiravir with highly p...

The present invention relates to an improved process for the preparation of 4-Phenylmorpholin-3-one with commercially viable and industrially applicable process in terms of good yield and purity.

ABSTRACT TITLE: “PROCESS FOR THE PREPARATION OF (3R,4R)-(1-BENZYL-4-METHYLPIPERIDIN-3-YL)-METHYLAMINE” The present invention relates to a process for preparation of (3R,4R)-(1-benzyl-4-methylpiperidin-3-yl)-methylamine (1) by employing novel compound of formula (4) and (5). The compound of formula (1) is a key...

ABSTRACT TITLE: “PROCESS FOR THE PREPARATION OF BILASTINE” The present invention relates to an improved, commercially viable, industrially advantageous and cost effective process for the preparation of Bilastine with good yield and purity

ABSTRACT “SYNTHESIS OF FAVIPIRAVIR” The present invention relates to a process for the preparation of Favipiravir. The present invention is also relates to an improved and commercially viable process of Favipiravir by using 6-fluoro-3-hydroxypyrazine-2-carbonitrile ammonia salt.

ABSTRACT Title: “ONE POT SYNTHESIS OF FAVIPIRAVIR” The present invention relates to a one pot process for the preparation of Favipiravir. The present invention is also relates to an improved, commercially viable, industrially advantageous, easier to handle and environmental friendly process for the preparation...

ABSTRACT Title: “PROCESS FOR THE PREPARATION OF FAVIPIRAVIR” The present invention relates to a process for the preparation of Favipiravir. The present invention is also relates to an improved, commercially viable, industrially advantageous, easier to handle and environmental friendly process for the preparati...

ABSTRACT “IMPROVED PROCESS FOR MOLNUPIRAVIR” The present invention relates to a process for the preparation of Molnupiravir. The present invention also relates to an improved and commercially viable process for preparation of Molnupiravir with high yield and purity.

TITLE: “AN IMPROVEDPROCESS FOR THE PREPARATION OF SUTEZOLID” The present invention relates to an improved, commercially viable and industrially advantageous process for the preparation of Sutezolid and its intermediates

TITLE: “A NOVEL PROCESS FOR THE PREPARATION OF SUTEZOLID ” A novel process for the preparation of Sutezolid and the present invention is also provides most economical and industrial applicable process.

The present invention relates to purification process of Obeticholic acid (I). The present invention further relates to crystalline forms of Obeticholic acid, which are useful to produce highly pure amorphous Obeticholic acid.

TITLE: “ONE POT PROCESS FOR THE PREPARATION OF DICYCLOHEXYL AMINE SALT OF 6-FLUORO-3-HYDROXY-2-PYRIDINE CARBONITRILE” The present invention relates to one pot process for the preparation of dicyclohexylamine salt of 6-fluoro-3-hydroxy-2-pyridine carbonitrile commercially viable and industrially applicable pro...

TITLE: CRYSTALLINE FORM XI OF RIFAXIMIN The present invention relates to a novel crystalline Form XI of Rifaximin and also relates to purification process of Rifaximin.

ABSTRACT TITLE: “AN IMPROVED PROCESS FOR PREPARATION OF BEMPEDOIC ACID” The present invention relates to an improved process for the preparation of Bempedoic acid (I), comprising hydrolyzing the compound of formula (4) with ionic liquid to obtain the compound of formula (5), which is converting to Bempedoic ac...

ABSTRACTTITLE: "A PROCESS FOR THE PREPARATION OF DABIGATRAN ETEXILATE AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF"The present invention is relates to a process for the preparation of Dabigatran etexilate and pharmaceutically acceptable salts thereof. The present invention is also relates to a p...

ABSTRACT Title: “IMPROVEED PROCESS FOR PREPARATION OF BEMPEDOIC ACID” The present invention relates to an improved, commercially viable and industrially advantageous process for the preparation of Bempedoic acid (I) with good yield and high purity using dicyclohexylammonium 2,2,14,14-tetramethyl-8-oxo pentadec...

ABSTRACT TITLE: “PROCESS FOR THE PREPARATION OF PROCESS FOR THE PREPARATION OF 4-(4-ISOPROPOXYBENZYL)-1-ISOPPROPYL-5-METHYL-1H-PYRAZOL-3(2H)-ONE” The present invention relates to a process for the preparation of 4-(4-Isopropoxybenzyl)-1-isoppropyl-5-methyl-1H-pyrazol-3(2H)-one of formula (I). ...

TITLE: CRYSTALLINE FORM I OF CAMOSTAT MESILATE The present invention relates to crystalline form I of Camostat mesilate. The present invention also relates to a purification process for preparing Camostat mesilate.

TITLE: PURIFICATION PROCESS OF STABLE FORM A LINAGLIPTIN The present invention relates to improved, commercially viable and industrially applicable purification process of stable form A Linagliptin with high purity and yield.

ABSTRACT TITLE: CRYSTALLINE FORM “P” OF BEMPEDOIC ACID The present invention relates to crystalline form “P” of Bempedoic acid. The present invention also relates to a purification process for preparing crystalline form “P” of Bempedoic acid with high purity and yield.

TITLE: CRYSTALLINE FORM I OF BUCILLAMINE The present invention relates to crystalline form I of Bucillamine. The present invention also relates to a purification process for preparing crystalline form I of Bucillamine.

ABSTRACT TITLE: NOVEL CRYSTALLINE FORM OF MIDODRINE HYDROCHLORIDE The present invention relates to purification process for Midodrine hydrochloride. And the present invention also relates to novel crystalline Form “OP” of Midodrine hydrochloride.

ABSTRACT “IMPROVED PROCESS FOR DAPAGLIFLOZIN PROPANE DIOL MONOHYDRATE” The present invention relates to an improved process for preparing (1S)-1,5-anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-D-glucitol(2S)-1,2-propanediol, hydrate i.e, Dapagliflozin Propanediol monohydrate (I), simple, efficient m...

ABSTRACT “PROCESS OF MOLNUPIRAVIR” The present invention relates to a process for preparation of Molnupiravir (1) by employing novel compound of formula (2), (3) and (4). The present invention is also relates to an improved and commercially viable process of Molnupiravir with high yield and purity. ...

ABSTRACT “SYNTHESIS OF BRIVARACETAM” The present invention relates to a novel compound of (S)-2-((Z)-((R)-4-propyldihydrofuran-2(3H)-ylidene) amino) butanamide and an improved, commercially viable process for preparation of Brivaracetam using (S)-2-((Z)-((R)-4-propyldihydrofuran-2(3H)-ylidene) amino) butanamide....

ABSTRACT “IMPROVED PROCESS FOR 2-DEOXY-D-GLUCOSE” The present invention relates to commercially, industrial applicable and improved process for the preparation of 2-Deoxy-D-glucose (I). The present invention is also provides simple, efficient more economical and eco-friendly process. ...

ABSTRACT “PROCESS FOR PREPARING ELAGOLIX” The present invention relates to a process for the preparation of Elagolix sodium comprising isolating of solid crystalline Form-P of compound (V). The present invention also relates to a solid crystalline Form-P of compound of formula (V). ...

ABSTRACT “IMPROVED PROCESS FOR TAFAMIDIS” The present invention relates to a process for the preparation of Tafamidis. The present invention is also relating to an improved and commercially viable process of Tafamidis with high yield.

ABSTRACT “IMPROVED PROCESS FOR THE PREPARATION OF ELAGOLIX” The present invention relates to an improved process for the preparation of Elagolix sodium with simple, high purity and good yield.

ABSTRACT TITLE: “PREPARATION OF SITAGLIPTIN PHOSPHATE MONOHYDRATE” The present invention relates to a process for the preparation of Sitagliptin phosphate monohydrate (I) from the novel compound of (2Z)-1-[5,6-dihydro-3-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazin-7(8H)-yl]-3-[[(1R)-1-phenylethyl]amino]-4-(2...

ABSTRACT Title: “A PROCESS FOR PREPARATION OF BEMPEDOIC ACID AND ITS INTERMEDIATES” The present invention relates to an improved, commercially viable and industrially advantageous process for the preparation of Bempedoic acid (I) with good yield and high purity via dicyclohexylamine salt of Bempedoic acid (5). T...

ABSTRACT “PROCESS FOR (R)-4-PROPYLDIHYDROFURAN-2(3H)-ONE” The present invention relates to an improved process for the preparation of (R)-4-propyldihydrofuran-2 (3H)-one (I), which is a key intermediate for the preparation of Brivaracetam. The present invention is also relating to a commercially viable and co...

ABSTRACT “IMPROVED PROCESS FOR TERIFLUNOMIDE” The present invention relates to a process for the preparation of Teriflunomide. The present invention is also relating to an improved and commercially viable process of Teriflunomide with high yield and high purity.

ABSTRACT “IMPROVED PROCESS FOR (R)-4-PROPYLDIHYDROFURAN-2(3H)-ONE” The present invention relates to a process for the preparation of (R)-4-propyldihydrofuran-2 (3H)-one (I), which is a key intermediate for the preparation of Brivaracetam. The present invention is also relating to an improved and commercially vi...

ABSTRACT “A PROCESS FOR THE PURIFICATION OF MOLNUPIRAVIR WITH SUBSTANTIALLY FREE FROM IMPURITIES” The present invention provides an efficient process for the purification of Molnupiravir with substantially free from impurities such as Dimethyl dioxol impurity (I), Acetyl impurity (II) and N-Hydroxycytidine impur...

ABSTRACT TITLE: “PROCESS FOR BEMPEDOIC ACID USING NOVEL INTERMEDIATES” The present invention relates to process for the preparation of Bempedoic acid (I) and the present invention further relates to a novel intermediate compounds of formulae (3) and (4) are used in the preparation of Bempedoic acid (I). ...

ABSTRACT “NOVEL PROCESS FOR THE PREPARATION OF FINERENONE” The present invention relates to a novel process for the preparation of Finerenone from the compound of formulae (IV), (VI), (VII) and (VIII).

“IMPROVED PROCESS FOR THE PREPARATION OF FINERENONE” The present invention provides an improved process for the preparation of Finerenone with high yield. It also relates to industrially viable process for the preparation of Finerenone (I).

ABSTRACT “IMPROVED PROCESS FOR THE PREPARATION OF 5-(2-FLUOROPHENYL)-1H-PYRROLE-3-CARBALDEHYDE” The present invention relates to an improved process for the preparation of 5-(2-Fluorophenyl)-1H-pyrrole-3-carbaldehyde (I) with high yield and purity.

ABSTRACT “IMPROVED PROCESS FOR 2-((1R,4R)-4-((TERT-BUTOXYCARBONYL) AMINO) CYCLOHEXYL) ETHYL METHANE SULFONATE” The present invention relates to an improved process for the preparation of 2-((1R,4R)-4-((tert-butoxycarbonyl) amino) cyclohexyl) ethyl methane sulfonate, which is used key intermediate for the pr...

ABSTRACT “NOVEL SYNTHESIS OF 5-(2-FLUOROPHENYL)-1H-PYRROLE-3-CARBALDEHYDE” The present invention relates to a process for the preparation of 5-(2-Fluorophenyl)-1H-pyrrole-3-carbaldehyde by using novel compound of formula (XIII) and (XIV).

ABSTRACT TITLE: PRODUCTION CRYSTALLINE FORMS OF RIFAXIMIN The present invention relates to an improved process for the preparation of mixed crystalline Rifaximin a and Rifaximin ß.

ABSTRACT “IMPROVED PROCESSES FOR THE PREPARATION OF ROXADUSTAT” The present invention relates to an improved process for the preparation of Roxadustat and also provided a process for preparation of pure crystalline Form A of Roxadustat.

ABSTRACT “CRYSTALLINE FORM P OF ISAVUCONAZONIUM SULFATE” The invention relates to a crystalline form P of Isavuconazonium Sulfate is characterized by an X-ray powder diffraction pattern having characteristic peaks at about 4.27, 7.26, 11.94 and 20.91 ± 0.2 degrees of two-theta. The invention also relates t...

ABSTRACT “PREPARATION OF 3'-AMINO-2'-HYDROXY-[1,1'-BIPHENYL]-3-CARBOXYLIC ACID” The present invention relates to a process for the preparation of 3'-amino-2'-hydroxy-[1,1'-biphenyl]-3-carboxylic acid with high yield and purity.

ABSTRACT “CRYSTALLINE FORM OF PHENYRAMIDOL HYDROCHLORIDE” The present invention relates to a crystalline form of Phenyramidol hydrochloride. The present invention also relates to process for the preparation of crystalline form of Phenyramidol hydrochloride with high purity and yield.

ABSTRACT TITLE: CRYSTALLINE FORM-OS OF ELTROMBOPAG FREE ACID. The present invention relates to crystalline Form-OS of Eltrombopag free acid (I). The present invention also relates to a purification process for preparing crystalline Form-OS of Eltrombopag free acid (I).

ABSTRACT “IMPROVED PROCESS FOR THE PREPARATION OF ELTROMBOPAG OLAMINE” The present invention relates to an improved process for the preparation of Eltrombopag Olamine and also relates to a process for the purification of Eltrombopag free acid.

ABSTRACT “IMPROVED PROCESSES FOR THE PREPARATION OF UPADACITINIB” The present invention relates to an improved process for the preparation of Upadacitinib with high yield and purity.

ABSTRACT “IMPROVED PROCESS FOR THE PREPARATION OF ELTROMBOPAG OLAMINE BY USING AMINE SALTS” The present invention relates to an improved process for the preparation of Eltrombopag Olamine by using amine salts and also relates to a process for the purification of Eltrombopag amine salts.

ABSTRACT “PREPARATION OF PYRIDINE-3-SULFONYL CHLORIDE” The present invention relates to a process for the preparation of Pyridine-3-sulfonyl chloride with high yield and purity.

ABSTRACT TITLE: PURIFICATION CRYSTALLINE FORM A OF VONOPRAZAN FUMARATE The present invention relates to a purification crystalline form A of Vonoprazan Fumarate with high purity.

ABSTRACT “IMPROVED PROCESSES FOR THE PREPARATION OF TAFAMIDIS” The present invention relates to an improved process for the preparation of Tafamidis. And also the present invention relates to a simple, cost effective, commercially viable and industrially applicable process of Tafamidis with high yield ...

ABSTRACT TITLE: “CRYSTALLINE FORM OF TRISODIUM SACUBITRIL VALSARTAN HYDRATE AND A PROCESS FOR PREPARATION THEREOF” The present invention relates to a crystalline Form P of a trisodium Sacubitril valsartan hydrate. Particularly, present invention relates to a process for the preparation of crystalline Form P of...

ABSTRACT “SOLID DISPERSION OF TRISODIUM SACUBITRIL VALSARTAN COMPLEX AND PROCESS FOR THE PREPARATION THEREOF” The present invention relates to an amorphous solid dispersion of trisodium Sacubitril valsartan complex with copovidone or colloidal silicon dioxide and process for preparation of amorphous solid dis...

ABSTRACT “PREPARATION OF 1-[(BENZYLOXY)CARBONYL]-4-ETHYL-2,5-DIHYDRO-1H-PYRROLE-3-CARBOXYLIC ACID” The present invention relates to a process for the preparation of 1-[(benzyloxy)carbonyl]-4-ethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid with high yield and purity.

ABSTRACT “PROCESS FOR 5-(2-FLUORO-3-METHOXYPHENYL)-1-(2-FLUORO-6-(TRIFLUOROMETHYL) BENZYL)-6-METHYLPYRIMIDINE-2,4(1H,3H)-DIONE” The present invention relates to an improved process for the preparation of 5-(2-fluoro-3-methoxyphenyl)-1-(2-fluoro-6-(trifluoromethyl) benzyl)-6-methylpyrimidine-2,4(1h,3h) dione (...

ABSTRACT “IMPROVED PROCESS FOR THE PREPARATION OF OZENOXACIN” The present invention relates to an improved process for the preparation of Ozenoxacin and also relates to a process for the purification of Ozenoxacin.

“AN IMPROVED PROCESS FOR THE PREPARATION OF 5-(2-FLUOROPHENYL)-1H-PYRROLE-3-CARBALDEHYDE” The present invention relates to an improved process for the preparation of 5-(2-Fluorophenyl)-1H-pyrrole-3-carbaldehyde by using novel compound of formula (XIIA), an intermediate in the synthesis of Vonoprazan Fumarate. ...

ABSTRACT “CRYSTALLINE FORM I OF CENOBAMATE” The present invention relates to crystalline Form I of Cenobamate. The present invention also relates to a process for the preparation of crystalline Form I of Cenobamate with high purity and yield.

TITLE: “SYNTHESIS OF 3'-AMINO-2'-HYDROXY-[1,1'-BIPHENYL]-3-CARBOXYLIC ACID” The present invention relates to a synthesis of 3'-amino-2'-hydroxy-[1,1'-biphenyl]-3-carboxylic acid (I).

ABSTRACT TITLE: CRYSTALLINE FORM I OF ETHACIZINE HYDROCHLORIDE The present invention relates to crystalline form I of Ethacizine hydrochloride. The present invention also relates to a purification process for preparing crystalline form I of Ethacizine hydrochloride.

“A PROCESS FOR THE PREPARATION OF 3-ETHYLBICYCLO[3.2.0]HEPT-3-EN-6-ONE” The present invention relates to a process for the preparation of 3-Ethylbicyclo[3.2.0]hept-3-en-6-one with high yield and purity, which is key intermediate for the preparation of Mirogabalin Besylate

ABSTRACT “AN IMPROVED PROCESS FOR PREPARATION OF DAPAGLIFLOZIN PROPANEDIOL MONOHYDRATE” The present invention relates to an improved process for preparing Dapagliflozin propanediol monohydrate, represented by formula (I). The invention also relates to the preparation of a substantially pure tetra acetyl inte...

“AN IMPROVED PROCESS FOR THE PREPARATION OF LINAGLIPTIN” The present invention relates to an improved process for the preparation of Linagliptin (I), comprising reacting the compound of formula (II) with compound of formula (III) in presence of base, solvent and phase transfer catalyst (PTC) to obtain compound o...

The present invention relates to improved methods for commercially preparing and separating compound 1-(2-chlorophenyl)-2-(2H-tetrazol-2-yl)ethanone (1a) from a reaction mixture containing compound 1-(2-chlorophenyl)-2-(2H-tetrazol-2-yl)ethanone (1a) and compound 1-(2-chlorophenyl)-2-(1H-tetrazol-2-yl)ethanone (1b),...

TITLE: IMPROVED PROCESS FOR THE PREPARATION OF PURE CRYSTALLINE FORM-I OF CRISABOROLE. The present invention relates to improved process for the preparation of pure crystalline Form-I of Crisaborole having purity of greater than 99.8%.

NOVEL PROCESS FOR THE PREAPARATION OF AMOROLFINE HYDROCHLORIDE” The present invention relates to a novel process for the preparation of Amorolfine hydrochloride (I). Furthermore, the invention pertains to novel compounds of formulae (IV) and (V), which are used in the preparation of Amorolfine hydrochloride (I) wit...

The present invention relates to a synthesis of butyl 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylate and also provided a purification of butyl 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylate.

TITLE: CRYSTALLINE FORM S1 OF TAPINAROF The present invention provides a crystalline Form S1 of Tapinarof. The present invention also relates to a process for preparing crystalline Form S1 of Tapinarof.

“A PROCESS FOR THE PREPARATION OF (3R,4R)-1-BENZYL-N,4-DIMETHYL PIPERIDIN-3-AMINE DIHYDROCHLORIDE (VI)” The present invention relates to a process for the preparation of (3R,4R)-1 Benzyl N,4 dimethylpiperidin 3 amine dihydrochloride (VI), a key intermediate in the synthesis of Tofacitinib citrate. The invention f...

AN IMPROVED PROCESS FOR THE PREPARATION OF LUMATEPERONE AND SALT THEREOF The present invention relates to an improved process for the preparation of Lumateperone of Formula (I) and salt thereof with high yield and purity.

ABSTRACT “AN IMPROVED PROCESS FOR THE PREAPARATION OF AMOROLFINE HYDROCHLORIDE” The present invention relates to an improved process for the preparation of Amorolfine hydrochloride (I). Furthermore, the invention pertains to novel compounds of formulae (VIa), which is used in the preparation of Amorolfine hydrochl...

TITLE: AN IMPROVED PROCESS FOR THE PREPARATION OF TAPINAROF AND ITS INTERMEDIATES The present invention relates to an improved process for the preparation of Tapinarof and a process for the preparation of Tapinarof intermediates.

Title: PROCESS FOR THE PREPARATION OF MIROGABALIN BESYLATE The present invention relates a process for the preparation of Mirogabalin Besylate with high yield and purity.

ABSTRACT “AN IMPROVED PROCESS FOR THE PREPARATION OF TEGOPRAZAN” The present invention relates to an improved process for the preparation of Tegoprazan, which provides high yield and high purity. Furthermore, the present invention provides an economical and technically simple process for the preparation of Teg...