Impliqué dans 17 réactions

6935

COC(=O)CCCCNC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #3879
title compound
Rendement 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)CCCCN.Cl
Reaction #44974
methyl 5-aminovalerate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(NOCCO)c1cc(CN2CCCCC2=O)c(F)c(F)c1Nc1ccc(I)cc1F
Reaction #49052
3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-piperidin-1-ylmethyl)-benzamide
Rendement 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)CCCCNC(=O)c1c(C)[nH]c(C=NN=C2C(=O)Nc3ccc(F)cc32)c1C
Reaction #338841
title compound
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(=O)CCCCNC(=O)c1cccc(C=C2C(=O)Nc3ccc(F)cc32)c1
Reaction #338883
title compound
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(=O)CCCCNC(=O)C(COC1CCCCO1)NS(=O)(=O)c1ccc(Cl)cc1
Reaction #353454
(RS)-2-(4-chlorobenzenesulfonylamino)-N-(4-methoxycarbonylbutyl)-3-(tetrahydropyran-2-yloxy)propanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
COC(=O)CCCCN.Cl
Reaction #579018
methyl 5-aminovalerate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
COC(=O)CCCCNC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #833407
title compound
Rendement 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_07
COC(=O)CCCCNC(=O)C(CSC(C)=O)Cc1ccccc1
Reaction #1527260
(±)-5-[[2-[(acetylthio)methyl]-1-oxo-3-phenylpropyl]amino]pentanoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_03
COC(=O)CCCCNC(=O)C=C1c2ccccc2-c2ccccc21
Reaction #2013368
title compound
Rendement 82.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
O=C(NOCCO)c1cc(CN2CCCCC2=O)c(F)c(F)c1Nc1ccc(I)cc1F
Reaction #2125832
3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-piperidin-1-ylmethyl)-benzamide
Rendement 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
O=C1CCCCN1Cc1ccnc(Nc2ccccc2)n1
Reaction #2192310
title compound
Rendement 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_08
COC(=O)CCCCN.Cl
Reaction #2196226
methyl 5-aminovalerate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_04
COC(=O)CCCCN.Cl
Reaction #2310557
methyl 5-aminovalerate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_05
COC(=O)CCCCNC(=O)c1c(-c2c(F)cccc2Cl)noc1C
Reaction #2315658
title compound
Rendement 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_07
COC(=O)CCCCN.Cl
Reaction #2322762
methyl 5-aminopentanoate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_05
COC(=O)CCCCNC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2500142
title compound
Rendement 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_01