ethyl bromopyruvate

O=C(O)c1coc2c1C(=O)CCC2
Reaction #995
4-oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1cn2c(Cl)cccc2n1
Reaction #5524
desired product
収率 67.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)c1csc(Nc2cnc(CNC(=O)OC(C)(C)C)c3c(OC)cc(OC)cc23)n1
Reaction #42928
2-[1-(tert-butoxycarbonylamino-methyl)-6,8-dimethoxy-isoquinolin-4-ylamino]thiazole-4-carboxylic acid ethyl ester
収率 42.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1csc(Nc2cnc(CNC(=O)OC(C)(C)C)c3cc(OC)c(OC)cc23)n1
Reaction #42949
2-[1-(tert-butoxycarbonylamino-methyl)-6,7-dimethoxy-isoquinolin-4-ylamino]thiazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1csc(-c2nc3c(C#N)c(C)c(-c4ccccc4)c(F)c3o2)n1
Reaction #45768
compound
収率 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1csc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)n1
Reaction #53345
title compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #58915
crystals
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CS(=O)(=O)O[C@@H]1C[C@@H](c2nc(C(=O)O)cs2)N(C(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #65553
(2S,4R)-2- (4-carboxythiazol-2-yl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl) pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)C1=CNCCc2c1[nH]c1ccccc21
Reaction #66190
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCOC(=O)C1=CNC(CC)Cc2c1[nH]c1ccccc21
Reaction #66198
2-Ethyl 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid n-propyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1coc(/C=C/c2ccccc2)n1
Reaction #71125
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1coc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)n1
Reaction #71880
title compound
収率 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1csc(C(C)C)n1
Reaction #80972
desired compound
収率 86.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1csc(N2CCOCC2)n1
Reaction #80980
desired compound
収率 55.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1csc(N(CC)CC)n1
Reaction #80992
desired compound
収率 140.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1csc(N2CCOCC2)n1
Reaction #82215
desired compound
収率 55.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1cc(C(=O)c2csc(Nc3ccc(Cl)cc3)n2)cc(OC)c1OC
Reaction #91501
(2-((4-Chlorophenyl)amino)thiazol-4-yl)(3,4,5-trimethoxyphenyl)methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)c1csc(Nc2ccc3[nH]ccc3c2)n1
Reaction #91522
2-(1H-indol-5-ylamino)thiazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)C1=C[n+]2cnc3ccccc3c2C1.[Br-]
Reaction #94197
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CCOC(=O)c1cc2c3ccccc3ncn2c1
Reaction #94198
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
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