Busqueda de Subestructura

4587

CC(=O)c1ccnc(Cl)c1
Reaction #2247
4-acetyl-2-chloro-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccnc(Cl)c1
Reaction #2248
4-acetyl-2-chloro-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=CC(=O)c1ccnc(Cl)c1
Reaction #2250
3-dimethylamino-1-(2-chloro-4-pyridyl)-2-propen-1-one
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cccc(Nc2nccc(-c3ccnc(Cl)c3)n2)c1
Reaction #2252
N-(3-trifluoromethyl-phenyl)-4-(2-chloro-4-pyridyl)-2-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cnccc1C(C)=O
Reaction #4453
3-methoxy-4-acetylpyridine
Rendimiento 46.3%DOI: 10.6084/m9.figshare.5104873.v1
Br.COc1cnccc1C(=O)CBr
Reaction #4454
α-bromo-3-methoxy-4-acetylpyridine hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCC(=O)c1ccncc1
Reaction #11584
titled compound
Rendimiento 87.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)c1ccncc1
Reaction #44692
Ethyl 3-oxo-3-(4-pyridinyl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)OCCO1
Reaction #57804
N-[4-chloro-2-(pyridine4-carbonyl)-phenyl]-4-(2-methyl[1,3]dioxolan-2-yl)-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1COC(C)(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)O1
Reaction #57805
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1OC(C)(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)O[C@@H]1C
Reaction #57806
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Br)cc1
Reaction #57807
4-Bromo-N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCCCC2)cc1
Reaction #57808
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCCC2)cc1
Reaction #57809
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCS(=O)(=O)CC2)cc1
Reaction #57810
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)C[C@H](C)O1
Reaction #57811
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCSCC2)cc1
Reaction #57812
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #57813
amine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCC2)cc1
Reaction #57814
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(-c2ccoc2)cc1
Reaction #57825
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
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