Inventor · disambiguated record
Bang-Chi Chen
Also filed as: CHEN BANG-CHI
27 granted patents·14 pending applications·177 citations·filing 1993–2015
96Inventor score
Top patents by PatentIndex Score
41 records- 0195US7396932B2Process for preparing 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-onesBRISTOL MYERS SQUIBB CO·Filed 2005·Granted Jul 8, 2008·24 cites·39 claims
- 0292US7652146B2Process for preparing 2-aminothiazole-5-carboxamides useful as kinase inhibitorsBRISTOL MYERS SQUIBB CO·Filed 2005·Granted Jan 26, 2010·13 cites·13 claims
- 0389US7605273B2Aryl-substituted pyrazole-amide compounds useful as kinase inhibitorsBRISTOL MYERS SQUIBB CO·Filed 2008·Granted Oct 20, 2009·8 cites·14 claims
- 0487US7396935B2Aryl-substituted pyrazole-amide compounds useful as kinase inhibitorsBRISTOL MYERS SQUIBB CO·Filed 2004·Granted Jul 8, 2008·15 cites·12 claims
- 0586US6812345B2HMG-CoA reductase inhibitors and methodBRISTOL MYERS SQUIBB CO·Filed 2003·Granted Nov 2, 2004·17 cites·12 claims
- 0684US8420811B2Tetrahydroisoquinolines and intermediates thereforLOBBEN PAUL·Filed 2009·Granted Apr 16, 2013·11 cites·2 claims
- 0784US7034151B2Process for preparing pyrrolotriazine kinase inhibitorsBRISTOL MYERS SQUIBB CO·Filed 2004·Granted Apr 25, 2006·17 cites·4 claims
- 0881US7304157B2Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-onesBRISTOL MYERS SQUIBB CO·Filed 2005·Granted Dec 4, 2007·3 cites·15 claims
- 0977US6562994B2Process for the preparation of N-(substituted phenyl)-3-alkyl-,aryl- and heteroarylsulfonyl-2-hydroxy-2-alkyl- and haloalkylpropanamide compoundsBRISTOL MYERS SQUIBB CO·Filed 2001·Granted May 13, 2003·8 cites·23 claims
- 1076US6414156B2Process for preparing azacycloalkanoylaminothiazolesBRISTOL MYERS SQUIBB CO·Filed 2000·Granted Jul 2, 2002·6 cites·34 claims
- 1175US6100395AReductive alkylation of secondary amines with hydrosilaneBRISTOL MYERS SQUIBB CO·Filed 2000·Granted Aug 8, 2000·7 cites·12 claims
- 1272US7388096B2Crystalline forms of a factor Xa inhibitorBRISTOL MYERS SQUIBB CO·Filed 2005·Granted Jun 17, 2008·3 cites·22 claims
- 1371US8304403B2Heterocyclic CETP inhibitorsSALVATI MARK E·Filed 2010·Granted Nov 6, 2012·2 cites·17 claims
- 1470US6639074B2Process for preparing azacycloalkanoylaminothiazolesBRISTOL MYERS SQUIBB CO·Filed 2002·Granted Oct 28, 2003·3 cites·7 claims
- 1570US2010016320A1Aryl-substituted pyrazole-amide compounds useful as kinase inhibitorsBRISTOL MYERS SQUIBB CO·Filed 2009·Application pending·0 cites
- 1667US6613911B2Process for preparing arylacetylaminothiazolesBRISTOL MYERS SQUIBB CO·Filed 2002·Granted Sep 2, 2003·2 cites·19 claims
- 1766US6392053B2Process for preparing arylacetylaminothiazolesBRISTOL MYERS SQUIBB CO·Filed 2000·Granted May 21, 2002·2 cites·26 claims
- 1864US5672698APreparation of 2',3'-didehydro-3'-deoxythymidine from 5-methyluridineBRISTOL MYERS SQUIBB CO·Filed 1994·Granted Sep 30, 1997·21 cites·13 claims
- 1963US7579472B2Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-onesBRISTOL MYERS SQUIBB CO·Filed 2007·Granted Aug 25, 2009·0 cites·7 claims
- 2062US7435821B2Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-onesBRISTOL MYERS SQUIBB CO·Filed 2007·Granted Oct 14, 2008·0 cites·16 claims
- 2160US6160134AProcess for preparing chiral cyclopropane carboxylic acids and acyl guanidinesBRISTOL MYERS SQUIBB CO·Filed 1999·Granted Dec 12, 2000·8 cites·15 claims
- 2259US6906192B2Processes for the preparation of acid derivatives useful as serine protease inhibitorsBRISTOL MYERS SQUIBB CO·Filed 2003·Granted Jun 14, 2005·1 cites·6 claims
- 2356US2013060027A1Tetrahydroisoquinolines and intermediates thereforBRISTOL MYERS SQUIBB CO·Filed 2012·Application pending·0 cites
- 2454US8350084B2Alpha-(N-sulfonamido)acetamide compound as an inhibitor of beta amyloid peptide productionBRISTOL MYERS SQUIBB CO·Filed 2011·Granted Jan 8, 2013·0 cites·1 claims
- 2553US6897321B2Process for preparing azacycloalkanoylaminothiazoles (LD 137e)BRISTOL MYERS SQUIBB CO·Filed 2003·Granted May 24, 2005·0 cites·4 claims
- 2653US2003216440A1Process for preparing arylacetylaminothiazolesFiled 2003·Application pending·0 cites
- 2751US8642576B2Heterocyclic CETP inhibitorsSALVATI MARK E·Filed 2012·Granted Feb 4, 2014·0 cites·14 claims
- 2851US2006041124A1Process for preparing pyrrolotriazine kinase inhibitorsCHEN BANG-CHI·Filed 2005·Application pending·0 cites
- 2949US2015191494A1Tetrahydroisoquinolines and intermediates thereforBRISTOL MYERS SQUIBB CO·Filed 2015·Application pending·0 cites
- 3049US2007219370A1Process for preparing n-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino] -5-thiazolecarboxamide and related metabolites thereofBRISTOL MYERS SQUIBB CO·Filed 2007·Application pending·0 cites
- 3148US2004024216A1HMG-CoA reductase inhibitors and methodFiled 2003·Application pending·0 cites
- 3245US2006069260A1Preparation of N-aryl pyridonesZHANG HUIPING·Filed 2005·Application pending·0 cites
- 3345US2006069085A1Preparation of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-onesZHAO RULIN·Filed 2005·Application pending·0 cites
- 3441US2005215795A1Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitorsCHEN BANG-CHI·Filed 2005·Application pending·0 cites
- 3540US2004180898A1Processes for preparing imidazoquinoxalinones, heterocyclic-substituted imidazopyrazinones, imidazoquinoxalines and heterocyclic-substituted imidazopyrazinesFiled 2003·Application pending·0 cites
- 3639US5466787AProcess for preparing AZTBRISTOL MYERS SQUIBB CO·Filed 1993·Granted Nov 14, 1995·3 cites·20 claims
- 3739US2002028826A1HMG-CoA reductase inhibitors and methodFiled 2001·Application pending·0 cites
- 3839US2002013334A1HMG-CoA reductase inhibitors and methodFiled 2001·Application pending·0 cites
- 3937US2006142319A1Pyridyl-substituted spiro-hydantoin crystalline forms and processCHEN BANG-CHI·Filed 2005·Application pending·0 cites
- 4036US5608049APreparation of d4T from 5-methyluridineBRISTOL MYERS SQUIBB CO·Filed 1995·Granted Mar 4, 1997·3 cites·13 claims
- 4131US6340752B1Deprotection and recrystallization processesBRISTOL MYERS SQUIBB CO·Filed 1998·Granted Jan 22, 2002·0 cites·10 claims
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