NBS

O=C(O)c1c(Br)[nH]c2c1C(=O)CCC2
Reaction #1005
2-bromo-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid
Yield 29.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1310
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1316
Compound I
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3C(C)=S)cc1
Reaction #1338
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccc(CBr)cc1
Reaction #1517
4-bromomethylbenzoic acid
Yield 65.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1[nH]c(-c2ccccc2)nc(C(F)(F)F)c1Br
Reaction #1542
5-bromo-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone
Yield 83.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1[nH]c(-c2ccccc2)nc(-c2ccccc2)c1Br
Reaction #1543
5-bromo-2,6-diphenyl-4(3H)-pyrimidinone
Yield 48.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(Br)C=C(Cl)C(F)=CN1
Reaction #1961
title compound
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)Oc1cc(-n2nc3n(c2=O)CCCC3Br)c(Cl)cc1Cl
Reaction #2062
title product
Yield 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)CNC(=O)COc1ccc(C(=O)CBr)cc1
Reaction #2319
methyl N-[4-(bromoacetyl)phenoxyacetyl]glycinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)c1ccc(S(=O)(=O)Nc2ncnc(OCCO)c2Br)cc1
Reaction #2405
N-[5-bromo-6-(2-hydroxyethoxy)pyrimidin-4-yl]-4-tert-butylbenzenesulfonamide
Yield 65.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NC(=O)c1cccc(CO)c1
Reaction #2545
title compound
Yield 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(N=C(c2ccccc2)c2ccccc2)c(CBr)c1
Reaction #2851
title compound
Yield 56.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Fc1ccc(Br)cc1CBr
Reaction #2876
title compound
Yield 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(CBr)c(Br)c1
Reaction #3066
ethyl 3-bromo-4-bromomethylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNCC(C)=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C
Reaction #3995
1-methylamino-2,5,9-trimethyl-11-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8,10-undecapentaene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)C(Br)c1ccccc1
Reaction #4069
title compound
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC=C(C(=O)OC)c1ccccc1CBr
Reaction #4071
colorless crystals
Yield 97.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1cc2c(cc1Br)N1CCc3cccc(c31)C(N1CCN(C)CC1)=N2
Reaction #4128
product
Yield 11.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=[N+]([O-])c1cc(Br)ccc1N1CCc2cc(Br)ccc21
Reaction #4131
product
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
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