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Cl.O=S(=O)(Cl)c1ccccn1

CC[C@@H]1Cc2[nH]ncc2[C@H](CC)N1S(=O)(=O)c1ccccn1
Reaction #44044
cis-4,6-Diethyl-5-(pyridin-2-ylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(I)c2c(c1OS(=O)(=O)c1ccccn1)CNC2=O
Reaction #49578
4-(2-pyridinesulfonyloxy)-5-methoxy-7-iodoisoindolinone
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(Br)cn1
Reaction #86331
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NCCO)c1ccc(Br)cn1
Reaction #86333
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCC(F)(F)CC(NS(=O)(=O)c3ccc(Cl)cn3)C2=O)c(OC)c1
Reaction #289842
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cc(OCCOC)cc(NS(=O)(=O)c3ccccn3)c2[nH]1
Reaction #591995
title compound
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ncccc1Cl
Reaction #1241715
3-Chloro-2-Pyridine Sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=N[C@@](c2cc(NS(=O)(=O)c3ccc(Cl)cn3)ccc2F)(C(F)F)[C@H]2C[C@H]2O1
Reaction #1613830
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CCC(F)(F)C[C@@H](NS(=O)(=O)c3ccc(Cl)cn3)C2=O)c(OC)c1
Reaction #1870598
5-Chloro-pyridine-2-sulfonic acid [(R)-1-(2,4-dimethoxy-benzyl)-5,5-difluoro-2-oxo-azepan-3-yl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(OCCOC)cc(NS(=O)(=O)c3ccccn3)c2[nH]1
Reaction #2047617
title compound
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(OCCOC)cc(NS(=O)(=O)c3ccccn3)c2[nH]1
Reaction #2082051
title compound
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCCN(Cc1ccc(-c2nccs2)cc1)S(=O)(=O)c1ccccn1
Reaction #2204662
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCCN(Cc1ccc(-n2cccn2)cc1)S(=O)(=O)c1ccccn1
Reaction #2204667
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1cccc(CN(Cc2ccc(-c3cccnc3)cc2)S(=O)(=O)c2ccccn2)c1
Reaction #2204681
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1cccc(CN(Cc2ccc(-n3cccn3)cc2)S(=O)(=O)c2ccccn2)c1
Reaction #2204684
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1cccc(CN(Cc2ccc(-c3cncnc3)cc2)S(=O)(=O)c2ccccn2)c1
Reaction #2204690
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1cccc(CN(Cc2ccc(-c3cncnc3)cc2)S(=O)(=O)c2ccccn2)c1
Reaction #2204693
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1cccc(CN(Cc2ccc3c(c2)OCCO3)S(=O)(=O)c2ccccn2)c1
Reaction #2204714
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1cccc(CN(Cc2ccc(-n3cccn3)cc2)S(=O)(=O)c2ccccn2)c1
Reaction #2204729
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1cccc(CN(Cc2ccc(-c3ncccn3)cc2)S(=O)(=O)c2ccccn2)c1
Reaction #2204752
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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