Busqueda de Subestructura

3624

CCOC(=O)c1ccc(Nc2ncc(C(=O)OCC)o2)nc1
Reaction #588
Rendimiento 67.2%
CCOC(=O)c1ccc(Cl)nc1
Reaction #1319
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(Cl)nc1
Reaction #6081
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3(C)C)nc1
Reaction #6082
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(Cl)nc1
Reaction #6655
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CC(C)(C)S3)nc1
Reaction #6656
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CC(C)(C)O3)nc1
Reaction #6657
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCOCC2)nc1
Reaction #60024
ethyl 6-morpholin-4-ylpyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1ccc(NCCN)nc1
Reaction #60032
tert-butyl 6-[(2-aminoethyl)amino]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccccc1
Reaction #60190
final product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccc(Cl)cc1Cl
Reaction #60191
final product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccc(C#N)cc1
Reaction #60192
final product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(NCCNc2ccc([N+](=O)[O-])cn2)cc1-c1ccccc1
Reaction #60217
ethyl 6-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)-4-phenylpyridine-3-carboxylate
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(Cl)nc1
Reaction #64626
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc(C(C)(C)C)cc2)nc1
Reaction #64636
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)C[C@H]2C)nc1
Reaction #70466
title compound
Rendimiento 71.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCN[C@@H](C)C2)nc1
Reaction #70483
desired compound
Rendimiento 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)COC(=O)c1ccc(Cl)nc1
Reaction #73527
2,2-dimethylpropyl 6-chloropyridine-3-carboxylate
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(F)c(Cl)nc1Cl
Reaction #76156
2,6-dichloro-5-fluoro nicotinic acid
Rendimiento 62.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(Cl)nc1
Reaction #80649
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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