5-bromothiophene-2-carboxylic acid

CC(C)(C)OC(=O)C(C)(C)NC(=O)c1ccc(Br)s1
Reaction #43379
tert.-butyl 2-[(5-bromo-thiophen-2-yl)-carbonylamino]-isobutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cc(NC(=O)[C@@H](Cc2c[nH]cn2)NC(=O)c2ccc(Br)s2)ccc1C(=O)N1CCCC1
Reaction #43384
5-bromo-thiophene-2-carboxylic acid-N-{(1R)-2-[1H-imidazol-4-yl]-1-[3-methyl-4-(pyrrolidin-1-yl-carbonyl)-phenylcarbamoyl]-ethyl}-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)NC(=O)c1ccc(Br)s1
Reaction #47852
amide
収率 83.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1c(-c2ccc(C(=O)O)s2)cc(C)cc1[N+](=O)[O-]
Reaction #177008
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NCC(NC(=O)c1ccc(Br)s1)c1ccccc1
Reaction #177737
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)NC(=O)c1ccc(Br)s1
Reaction #181331
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cl)c1ccc(Br)s1
Reaction #187356
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(Br)s1
Reaction #265650
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(Cl)c1ccc(Br)s1
Reaction #284777
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)c1ccc(-c2ccoc2)s1
Reaction #315102
solid
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C(Nc1nc(CC(=O)N2CCN(CC(=O)N3CCCC3)CC2)cs1)c1ccc(Br)s1
Reaction #368941
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cn1nccc1-c1ccc(C(=O)O)s1
Reaction #403839
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Cl)c1ccc(Br)s1
Reaction #433136
5-bromo-2-thiophenecarbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
COc1ccc(NC(=O)c2ccc(Br)s2)cc1N1CCN(C)CC1
Reaction #442916
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
COc1c(-c2ccc(C(=O)O)s2)cccc1[N+](=O)[O-]
Reaction #471509
5-(2-methoxy-3-nitro-phenyl)thiophene-2-carboxylic acid
収率 85.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
COc1c(-c2ccc(C(=O)O)s2)cc(C)cc1[N+](=O)[O-]
Reaction #471524
5-(3-nitro-2-methoxy-5-methyl-phenyl)thiophene-2-carboxylic acid
収率 73.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(Nc1cc(NC(=O)c2c(Cl)cccc2Cl)ccn1)c1cnc(Br)s1
Reaction #537049
desired product
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CC(C)(C)OC(=O)c1ccc(Br)s1
Reaction #567510
title compound
収率 94.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
O=C(Cl)c1ccc(Br)s1
Reaction #573325
5-bromo-2-thiophenecarbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
Cc1ccc(C(=O)NC2CC2)cc1NC(=O)c1ccc(Br)s1
Reaction #632108
5-Bromo-N-(5-(cyclopropylcarbamoyl)-2-methylphenyl)thiophene-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
1 ページ次のページ