子结构搜索

13928

N#Cc1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4ccccc4s3)C2=O)c1
Reaction #2842
title compound
收率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(O)c(CN2CCC(NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #2855
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4nc(Cl)ccc4s3)C2=O)c1
Reaction #2858
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4ccc(Cl)nc4s3)C2=O)c1
Reaction #2860
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(O)c(CN2CC[C@H](NS(=O)(=O)c3cc4nc(Cl)ccc4s3)C2=O)c1
Reaction #2861
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N)c(CN2CC[C@H](NS(=O)(=O)c3cc4nc(Cl)ccc4s3)C2=O)c1
Reaction #2862
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(CN2CC[C@H](NS(=O)(=O)c3cc4nc(Cl)ccc4s3)C2=O)cs1
Reaction #2863
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(CN2CC[C@H](NS(=O)(=O)c3ccc(-c4ccc(Cl)s4)s3)C2=O)c1
Reaction #2865
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(CN2CC[C@H](NS(=O)(=O)c3cc4ccccc4s3)C2=O)ccc1N
Reaction #2866
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Cl)c1ccc(-c2cccnc2)s1
Reaction #2868
title product
收率 79.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #2869
crude product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(O)c(CN2CC[C@H](NS(=O)(=O)c3cc4ccc(Cl)cc4s3)C2=O)c1
Reaction #2873
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(F)c(CN2CC[C@H](NS(=O)(=O)c3ccc(-c4cccnc4)s3)C2=O)c1
Reaction #2877
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(-c2ccco2)c2cnn(Cc3cccc(-c4ccsc4S(N)(=O)=O)c3)c2n1
Reaction #8391
title compound
收率 22.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8424
hydrochloride salt
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]([C@@H](CO)NS(=O)(=O)c1ccc(Cl)s1)C(F)(F)F
Reaction #45306
5-Chloro-N-[(1S,2S)-3,3,3-trifluoro-1-(hydroxymethyl)-2-methylpropyl]thiophene-2-sulfonamide
收率 100.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(NS(=O)(=O)c4cccs4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45514
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3cc4ccccc4s3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49435
4-(benzothiophene-2-sulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc2[nH]nc(-c3cc4ccccc4[nH]3)c2c1)c1cccs1
Reaction #53718
solid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NS(=O)(=O)c1cccs1
Reaction #53774
product
DOI: 10.6084/m9.figshare.5104873.v1
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