Busqueda de Subestructura

1135397

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Reaction #47909
desired Compound 5
Rendimiento 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cn2)C1
Reaction #179695
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1cc(Br)cnc1Cl
Reaction #209780
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1
Reaction #211628
DOI: 10.1039/C8SC04228D
CSc1nc2c(c(Nc3ccc(C(F)(F)F)cc3)n1)CCN(c1ncccc1S(C)(=O)=O)C2
Reaction #237940
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(Nc2ncnc3c2CCN(c2ncccc2S(C)(=O)=O)C3)cc1
Reaction #280068
DOI: 10.1039/C8SC04228D
CC(=O)Nc1nc(C)c(-c2cnc(Cl)c(S(C)(=O)=O)c2)s1
Reaction #339879
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cc(Br)cnc1Cl
Reaction #339881
5-bromo-2-chloro-3-methylsulfonylpyridine
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1nc(C)c(-c2cnc(Cl)c(S(C)(=O)=O)c2)s1
Reaction #370314
DOI: 10.1039/C8SC04228D
CC(=O)N1CCN(c2ccc(NC(=O)Cc3cnc(-c4ccnc(C)c4)c(S(C)(=O)=O)c3)nc2)CC1
Reaction #386803
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #400396
DOI: 10.1039/C8SC04228D
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Reaction #622536
desired Compound 5
Rendimiento 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Cc1cnc(Cl)c(S(C)(=O)=O)c1
Reaction #679403
tert-butyl 2-(6-chloro-5-(methylsulfonyl)pyridin-3-yl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCN(c2ccc(NC(=O)Cc3cnc(Cl)c(S(C)(=O)=O)c3)nc2)CC1
Reaction #679404
N-(5-(4-acetylpiperazin-1-yl)pyridin-2-yl)-2-(6-chloro-5-(methylsulfonyl)pyridin-3-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCN(c2ccc(NC(=O)Cc3cnc(-c4ccnc(C)c4)c(S(C)(=O)=O)c3)nc2)CC1
Reaction #679405
N-(5-(4-acetylpiperazin-1-yl)pyridin-2-yl)-2-(2′-methyl-3-(methylsulfonyl)-2,4′-bipyridin-5-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cccnc1N1CCc2ncnc(Nc3ccc(C(F)(F)F)nc3)c2C1
Reaction #906661
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(Nc2ncnc3c2CCN(c2ncccc2S(C)(=O)=O)C3)cc1
Reaction #1058381
title compound
Rendimiento 48.7%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #1058382
desired compound
Rendimiento 49.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cccnc1N1CCc2c(ncnc2Nc2ccc(OC(F)F)cc2)C1
Reaction #1058393
title compound
Rendimiento 63.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)c1cccnc1N1CCc2c(ncnc2Nc2ccc(C(F)(F)F)cc2)C1
Reaction #1058397
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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