bromoacetyl bromide

O=C(CBr)NC1CCCOc2ccccc21
Reaction #1049
compound ( 8 )
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cccc(Cc2ccccc2)c1NC(=O)CBr
Reaction #1053
2-benzyl-1-(2-bromoacetylamino)-6-methylbenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CBr)N1CCCOc2ccccc21
Reaction #1055
5-(2-bromoacetyl)-2,3,4,5-tetrahydro-1,5-benzoxazepine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cccc(C)c1NC(=O)CBr
Reaction #1058
N-(2,6-dimethylphenyl)-2-bromoacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CBr)Nc1ccccc1
Reaction #1059
N-phenyl-2-bromoacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)c1cccc(C(C)C)c1NC(=O)CBr
Reaction #1060
N-(2,6-diisopropylphenyl)-2-bromoacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=C(c1ccccc1)N(C)C(=O)CBr
Reaction #1061
N-methyl-N-(1-phenylvinyl)-2-bromoacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CBr)NC1CCCCCC1
Reaction #3058
solid
Выход 89.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CBr)NOCc1ccccc1
Reaction #3059
title compound
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3060
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NN1CCN(C(=O)CBr)C1=O
Reaction #4214
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(c1ccccc1)c1cccc2c1N(C(=O)CBr)CCO2
Reaction #6460
4-bromoacetyl-5-benzoyl-3,4-dihydro-2H-1,4-benzoxazine
Выход 69.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)OC(=O)CC[C@H](NC(=O)CBr)C(=O)N[C@@H](CCC(=O)OCC[Si](C)(C)C)C(=O)OC(C)(C)C
Reaction #9808
product
Выход 78.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCc1nc(CC)c2c(=O)[nH]c(-c3cc(C(=O)CBr)ccc3OCC)nn12
Reaction #11365
2-[5-(2-Bromoacetyl)-2-ethoxyphenyl]-5-ethyl-7-propyl-3H-imidazo[5,1-f][1,2,4]-triazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1ccc(C(=O)CBr)cc1-c1nn2c(C3CCCCCC3)nc(C)c2c(=O)[nH]1
Reaction #11366
desired product
Выход 66.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)c1oc2c3c(ccc2c(=O)c1-c1ccc(Cl)cc1)NC(=O)CO3
Reaction #42789
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(CBr)Nc1ccc(Cl)cc1
Reaction #46786
2-Bromo-N-(4-Chloro-phenyl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(CBr)Nc1ccc(Cl)cn1
Reaction #46787
2-Bromo-N-(5-Chloro-pyridin-2-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(C(=O)CBr)ccc3OCC)nc12
Reaction #50229
title compound
Выход 78.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CSc1cc(C)nc(SC)c1NC(=O)CBr
Reaction #51161
2-bromo-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]acetamide
Выход 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Страница 1Далее