Inventor

KANAMARLAPUDI RAMANAIAH C

US13 patents

⚠️ This page may combine multiple inventors who share the name “KANAMARLAPUDI RAMANAIAH C”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

LEXICON PHARMACEUTICALS INC

7 patents

US6951946B2Oct 4, 2005

Modified safe and efficient process for the environmentally friendly synthesis of imidoesters

LEXICON PHARMACEUTICALS INC2 citations60

US6642390B2Nov 4, 2003

One step synthesis of 1,2,3-triazole carboxylic acids

LEXICON PHARMACEUTICALS INC3 citations57

US7919618B2Apr 5, 2011

Synthesis of piperazines, piperidines and related compounds

LEXICON PHARMACEUTICALS INC0 citations49

BEDNARZ MARK S

3 patents

US8193204B2Jun 5, 2012

Solid forms of (S)-ethyl 2-amino-3-(4-(2-amino-6-((R)-1- (4-chloro-2-(3-methyl-1H-pyrazol-1-YL)phenyl)2,2,2-trifluoroethoxy)-pyrimidin-4-YL)phenyl)propanoate and methods of their use

BEDNARZ MARK S3 citations57

US8653094B2Feb 18, 2014

Solid forms of (S)-ethyl 2-amino-3-(4-(2-amino-6-((R)-1-(4-chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethoxy)-pyrimidin-4-yl)phenyl)propanoate and methods of their use

BEDNARZ MARK S1 citations47

US8575362B2Nov 5, 2013

Methods of preparing 4-phenyl-6-(2,2,2-trifluoro-1-phenylethoxy)pyrimidine-based compounds

BEDNARZ MARK S1 citations47

KANAMARLAPUDI RAMANAIAH C

2 patents

US9085788B2Jul 21, 2015

Process for preparing an enantiomerically enriched, deuterated secondary alcohol from a corresponding ketone without reducing deuterium incorporation

KANAMARLAPUDI RAMANAIAH C2 citations57

US9074233B2Jul 7, 2015

Process for preparing an enantiomerically enriched, deuterated secondary alcohol from a corresponding ketone without reducing deuterium incorporation

KANAMARLAPUDI RAMANAIAH C1 citations46

BURGOON HUGH ALFRED

1 patent

US8450532B2May 28, 2013

Compounds useful in the preparation of tryptophan hydroxylase inhibitors

BURGOON HUGH ALFRED1 citations58

KANAMARLAPUDI RAMANAIAH C

LEXICON PHARMACEUTICALS INC

Large scale synthesis of 1,2,4- and 1,3,4-oxadiazole carboxylates

1-phenyl-1H-pyrazole-based compounds

Process for preparing 5-alkyl-7H-pyrrolo[2,3-d] pyrimindine-2-ols

Process for the preparation of substituted phenylalanines

Modified safe and efficient process for the environmentally friendly synthesis of imidoesters

One step synthesis of 1,2,3-triazole carboxylic acids

Synthesis of piperazines, piperidines and related compounds

BEDNARZ MARK S

Solid forms of (S)-ethyl 2-amino-3-(4-(2-amino-6-((R)-1- (4-chloro-2-(3-methyl-1H-pyrazol-1-YL)phenyl)2,2,2-trifluoroethoxy)-pyrimidin-4-YL)phenyl)propanoate and methods of their use

Solid forms of (S)-ethyl 2-amino-3-(4-(2-amino-6-((R)-1-(4-chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethoxy)-pyrimidin-4-yl)phenyl)propanoate and methods of their use

Methods of preparing 4-phenyl-6-(2,2,2-trifluoro-1-phenylethoxy)pyrimidine-based compounds

KANAMARLAPUDI RAMANAIAH C

Process for preparing an enantiomerically enriched, deuterated secondary alcohol from a corresponding ketone without reducing deuterium incorporation

Process for preparing an enantiomerically enriched, deuterated secondary alcohol from a corresponding ketone without reducing deuterium incorporation

BURGOON HUGH ALFRED

Compounds useful in the preparation of tryptophan hydroxylase inhibitors