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3659

CCc1cccc(C)c1S(=O)(=O)c1nn(C(=O)N(CC)CC)c(SC)c1Cl
Reaction #49888
title compound
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1ccc2c(c1)C(CNc1ccccc1)=CC(C)(C)N2
Reaction #54048
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(Nc2nccc(-c3ccc(SCCCCO)cc3)n2)cc1)N1CCN(C(=O)c2ccco2)CC1
Reaction #61737
[4-(Furan-2-carbonyl)-piperazin-1-yl]-(4-{4-[4-(4-hydroxybutylsulfanyl)phenyl]pyrimidin-2-ylamino}phenyl)methanone
Выход 9.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNC[C@@H]1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67183
2-METHYL-N-{[(2R)-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}PROPAN-1-AMINE
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNC[C@H]1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67184
2-METHYL-N-{[(2S)-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}PROPAN-1-AMINE
DOI: 10.6084/m9.figshare.5104873.v1
COCCNCC1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67199
2-METHOXY-N-{[7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}ETHANAMINE
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNCC1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67200
2-METHYL-N-{[7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}PROPAN-1-AMINE
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc2c(c1)OC(CO)CO2
Reaction #67263
title compound
Выход 182.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC2COc3ccc(S(C)(=O)=O)cc3O2)cc1
Reaction #67264
title compound
Выход 74.6%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc2c(c1)O[C@H](CO)CO2
Reaction #67268
title compound
Выход 78.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC[C@@H]2COc3ccc(S(C)(=O)=O)cc3O2)cc1
Reaction #67269
title compound
Выход 87.5%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc2c(c1)O[C@@H](CO)CO2
Reaction #67273
title compound
Выход 213.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC[C@H]2COc3ccc(S(C)(=O)=O)cc3O2)cc1
Reaction #67274
[(2R)-7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL 4-METHYLBENZENESULFONATE
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1cccc(Sc2ccnc(Nc3cc(OC)c(OC)c(OC)c3)n2)c1
Reaction #168895
product
Выход 14.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)Nc1ccc(Sc2ccnc(Cl)n2)cc1
Reaction #168905
product
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)Nc1ccc(Nc2nccc(Sc3ccc(OC)cc3)n2)cc1
Reaction #168907
product
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)NCc1ccc(Sc2ccnc(Nc3ccc(N4CCOCC4)cc3)n2)cc1
Reaction #168908
product
Выход 27.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)NCc1cccc(Sc2ccnc(Nc3ccc(N4CCOCC4)cc3)n2)c1
Reaction #168909
product
Выход 31.3%DOI: 10.6084/m9.figshare.5104873.v1
BrCc1cccc(Sc2ccnc(Nc3ccc(N4CCOCC4)cc3)n2)c1
Reaction #168911
product
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1cn(Cc2cccc(Sc3ccnc(Nc4ccc(N5CCOCC5)cc4)n3)c2)cn1
Reaction #168912
product
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1
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