The present invention relates to an industrially feasible and economically viable process for the preparation of 3-aryloxy-3-phenylpropylamine and salt of formula I thereof.

The present invention relates to an industrially feasible and economically viable process for the preparation of l-(2,3-dichloro-phenyl)piperazine and its salt of formula I thereof.

The present invention relates to an industrially feasible process for preparation of substantially pure Lurasidone base of formula la and its conversion to pharmaceutically acceptable salts such as hydrochloride salt and the like in significantly high yields and purity.

The present invention relates to an industrially feasible and economically viable process for the preparation of fluvoxamine maleate of formula I.

The present invention relates to an improved and industrially applicable process for the preparation of aripiprazole and its crystal form of formula I thereof.

The present invention relates to an industrially feasible and economically viable process for the preparation of methylphenidate hydrochloride of formula 1 and its intermediates thereof.

The present invention relates to an improved process for the preparation of Memantine hydrochloride of formula (1). Memantine hydrochloride is used in the treatment of Alzheimer"s and Parkinson"s disease.

The present invention relates to an improved process for the preparation of Dexmethylphenidate hydrochloride of formula (A). More particularly, the present invention relates to an improved process for the preparation of Dexmethylphenidate hydrochloride of formula (A) and its intermediate d-threo ritalinic acid hydro...

The present invention relates to an industrially feasible and economically viable process foT the preparation of nebivolol hydrochloride of formula I thereof.

The present invention relates to a process for the preparation of d-threo-ritalinic acid salt thereof. More particularly, the present invention relates a process for the preparation of d-threo-ritalinic acid salt via novel organic salts of intermediate thereof.

The  present  invention  relates  to  an  industrially  viable  and  environmentally advantageous process for the preparation of levomepromazine maleate.

ABSTRACT The present invention relates to an industrially feasible and economically viable process for the preparation of (lS,2R)-3-[[4-aminophenyl)-suifonyi](2-methylpropy!)amino]-2-hydroxy-l-(phenyl-methyl)propyl] amine of formula I and its salt thereof and optionally converting it to HIV-protease inhibitors like...

The present invention relates to an industrially feasible and economically viable process for the preparation of flupirtine maleate of formula I thereof.

ABSTRACT “Novel process for preparation of crystalline form of Pirfenidone” The present invention provides Novel process for preparation of a process for purification of Pirfenidone involving treating Pirfenidone with a quaternary ammonium salt. The present invention further provides a novel process for the pr...

The present invention relates to an industrially applicable process for kinetic resolution of racemic mixture of alcohol such as a mixture of (R) - and (S) - hydroxyl compounds. More particularly, the present invention relates to an industrially applicable process for separation of Eslicarbazepine from a racemic mix...

An Improved process for the preparation of Ticagrelor The present invention provides an improved process for the preparation of Ticagrelor. The improved process comprises of preparing compound of formula III by reacting compound of formula I and formula II or a salt thereof in presence of a base and a non-polar org...

The present invention provides improved isolation process for preparation of Maraviroc intermediate with high purity. The present invention further provides an improved process for preparation of Maraviroc compound of formula I with high purity.

The present invention provides an improved process for the preparation of Bempedoic acid compound of formula I and its intermediates having high purity and high yield. Further present invention provides process for purification of Bempedoic acid compound of formula I. Dated this 8th day of November, 2021 ...

The present invention relates to a process for the preparation of Anti influenza drug Favipiravir. The process being developed is one-pot synthesis which avoids isolation of intermediate compounds that are formed during the synthesis of Favipiravir. The present invention also provides a novel purification process wh...

The present invention provides an alternative approach for the preparation of Miglustat compound of formula IV and its intermediates having high purity. In particular, the present invention provides a process for the preparation of Miglustat through the tetra-O-protected 1-D-gluco-deoxynojirimycin or the tetra-O-pro...

The present invention provides a process for the preparation of enantiomerically pure (4R)-1-Methyl-4-(1-methylethenyl)-2-cyclohexen-1-ol compound of formula II, an intermediate in the synthesis of Cannabidiol. Further, the present invention relates to a process for the preparation of enantiomerically pure (4R)-2-(d...