Busqueda de Subestructura

20236

Nc1nn(CCCN2CCCC2)c2ccc(Cl)cc12
Reaction #572067
1-(3-pyrrolidinopropyl)-3-amino-5-chloroindazole
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nn(CCCN2CCCC2)c2ccccc12
Reaction #572088
1-(3-pyrrolidinopropyl)-3-aminoindazole
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C2C3=C(CCCC3=O)N(c3cccc(C(F)(F)F)c3)C(=O)N2CCCN2CCCC2)cc1
Reaction #604425
4-(1-(3-(Trifluoromethyl)phenyl)-2,5-dioxo-3-(3-(pyrrolidin-1-yl)propyl)-1,2,3,4,5,6,7,8-octahydroquinazolin-4-yl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nn(CCCN2CCCC2)c2ccc(Cl)cc12
Reaction #667344
1-(3-pyrrolidinopropyl)-3-amino-5-chloroindazole
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nn(CCCN2CCCC2)c2ccccc12
Reaction #667363
1-(3-pyrrolidinopropyl)-3-aminoindazole
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Br)cc1)C(Br)CC(=O)N1CCCC1C(=O)O
Reaction #757669
DOI: 10.1039/C8SC04228D
CC(=O)SC(CC(=O)N1CCCC1C(=O)O)C(=O)c1ccc(Br)cc1
Reaction #904341
DOI: 10.1039/C8SC04228D
COC(=O)[C@@H]1CCCN1C(=O)CC(Br)C(=O)c1ccc(Br)cc1
Reaction #990624
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CCCN1C(=O)CC(SC(C)=O)C(=O)c1ccc(Br)cc1
Reaction #990625
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Br)cc1)C(Br)CC(=O)N1CCC[C@H]1C(=O)O
Reaction #990627
1-[3-(4-Bromobenzoyl)-3-bromopropionyl]-L-proline
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SC(CC(=O)N1CCC[C@H]1C(=O)O)C(=O)c1ccc(Br)cc1
Reaction #990628
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)C(CC(=S)N1CCC[C@H]1C(=O)O)C(=O)c1ccc(Br)cc1
Reaction #990629
1-[3-(4-Bromobenzoyl)-3-benzoylthiopropionyl]-L-proline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CC2(CCN(c3ccc(OCCCN4CCC[C@H]4C)cc3)CC2)OCC1=O
Reaction #1183004
4-isopropyl-9-(4-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}phenyl)-1-oxa-4,9-diazaspiro[5,5]undecan-3-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1COC2(CCN(c3ccc(OCCCN4CCCC4)cc3)CC2)CN1Cc1ccccc1
Reaction #1183006
4-benzyl-9-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]-1-oxa-4,9-diazaspiro[5,5]undecan-3-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCCN1C(=O)CC(Br)C(=O)c1ccc(Br)cc1
Reaction #1321649
DOI: 10.1039/C8SC04228D
COc1cc2c(=O)n(-c3ccc(OCCCN4CCCC4)cc3)c(C)nc2cn1
Reaction #2199041
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Br.BrCCCN1CCCC1
Reaction #2283790
entitled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nsc(NC(=O)c2nc(Sc3nncn3C)ccc2Sc2ccc(OCCCN3CCCC3)cc2)n1
Reaction #2283791
entitled compound
Rendimiento 16.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCCN1C(=O)CC(SC(C)=O)C(=O)c1ccc(Br)cc1
Reaction #2411681
DOI: 10.1039/C8SC04228D
COc1cc2c(=O)n(-c3ccc(OCCCN4CCCC4)cc3)c(C)nc2cn1
Reaction #2474151
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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