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180490

CCOC(=O)c1cn(C)c2c(C)c(C=O)sc2c1=O
Reaction #51893
solid
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(C)c2c(C)c(CO)sc2c1=O
Reaction #51894
solid
Ausbeute 94.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CO)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51895
title compound
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CCl)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51896
title compound
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)CC(O)c2ccc(O)cc2)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51897
title compound
Ausbeute 77.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)OP(C)(=O)c2ccccc2)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51898
[[(6-{[(4-chlorobenzyl)amino]carbonyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridin-2-yl)methyl](methyl)amino]methyl(phenyl)phosphinic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc2c(C)c(CO)sc2c1O
Reaction #51899
title compound
Ausbeute 59.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CO)sc2c(O)c(C(=O)NCc3ccc(Cl)cc3)cnc12
Reaction #51900
title compound
Ausbeute 92.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CO)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(CC(N)=O)c12
Reaction #51901
title compound
Ausbeute 56.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CCl)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(CC(N)=O)c12
Reaction #51902
title compound
Ausbeute 101.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)CC(O)c2ccco2)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(CC(N)=O)c12
Reaction #51903
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)C[C@@H](O)c2ncccn2)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51904
title compound
Ausbeute 41.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)CC(O)c2ccc[n+]([O-])c2)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51905
titled compound
Ausbeute 59.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(CCO)CC(O)c2ccccc2)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51906
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)CC(O)c2ccc3c(c2)OCCO3)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51907
titled compound
Ausbeute 73.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CO)sc2c(O)c(C(=O)NCc3ccc(F)cc3)cnc12
Reaction #51908
title compound
Ausbeute 85.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CO)sc2c(=O)c(C(=O)NCc3ccc(F)cc3)cn(C)c12
Reaction #51909
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CCl)sc2c(=O)c(C(=O)NCc3ccc(F)cc3)cn(C)c12
Reaction #51910
N-(4-fluorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)C[C@@H](O)c2cnccn2)sc2c(=O)c(C(=O)NCc3ccc(F)cc3)cn(C)c12
Reaction #51911
title compound
Ausbeute 22.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(C)c2c(C)csc2c1=O
Reaction #51912
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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