Substructure Search

1172920

CCOC(=O)CNc1ncc(F)cc1N
Reaction #562
Yield 0.0%
—
Reaction #40585
solid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NS(=O)(=O)c2ccc3ncsc3c2)c(Br)n1
Reaction #40586
expected product
Yield 35.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc(-c3ccccc3)c(Cl)c2)c(C(=O)OC(C)(C)C)c1
Reaction #70337
tert-Butyl 2-(5-chloro-6-phenylpyridin-3-ylamino)-5-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)COc1cccnc1Br
Reaction #78407
2-bromo-3-(2,2,2-trifluoroethoxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N)c(Br)n1
Reaction #81800
title compound
Yield 70.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=O)c2cccnc2Cl)c(Br)n1
Reaction #81801
product
Yield 95.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(C)C(=O)c2cccnc2Cl)c(Br)n1
Reaction #81802
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ncccc1C(=O)N(C)c1ccc(OC)nc1Br
Reaction #81803
title compound
Yield 77.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1c2ncccc2C(=O)N(C)c2ccc(OC)nc21
Reaction #81804
5,11-dihydro-11-ethyl-2-methoxy-5-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
Yield 47.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)c(N)c(Br)n1
Reaction #81808
title compound
Yield 73.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)c(NC(=O)c2cccnc2Cl)c(Br)n1
Reaction #81809
title compound
Yield 84.6%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ncccc1C(=O)Nc1c(C)cc(OC)nc1Br
Reaction #81810
title compound
Yield 44.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN1c2ncccc2C(=O)Nc2c(C)cc(OC)nc21
Reaction #81811
5,11-dihydro-11-ethyl-2-methoxy-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
Yield 47.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccnc(Br)c1[N+](=O)[O-]
Reaction #88236
title compound
Yield 71.8%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ncc(Cl)cc1[N+](=O)[O-]
Reaction #158178
5-chloro-3-nitropyridine-2-carboxaldehyde
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)cnc(C=O)c1[N+](=O)[O-]
Reaction #158181
5-chloro-4-methyl-3-nitropyridine-2-carboxaldehyde
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(S(=O)(=O)Nc2cc(Cl)cnc2Br)cc1
Reaction #163164
sulfonamide
Yield 66.4%DOI: 10.6084/m9.figshare.5104873.v1
COCN(c1cc(Cl)cnc1Br)S(=O)(=O)c1ccc(C(C)(C)C)cc1
Reaction #163166
desired product
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(S(=O)(=O)Nc2cc(Cl)cnc2-n2ncc3ncccc32)cc1
Reaction #163168
4-tert-butyl-N-(5-chloro-2-pyrazolo[4,3-b]pyridin-1-yl-pyridin-3-yl)-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
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