Recherche de Sous-structure

413997

CC(C)(C)OC(=O)N1CCC(CNS(=O)(=O)c2ccc(Cl)cc2)CC1
Reaction #162289
product
Rendement 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](C(N)=O)N(CC1CCN(C(=O)OC(C)(C)C)CC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #594489
solid
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](C(N)=O)N(CC1CCNCC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #594490
solid
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(C(N)=O)N(CC1CCNCC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #902530
DOI: 10.1039/C8SC04228D
CC(C)CC(C(N)=O)N(CC1CCN(C(=O)OC(C)(C)C)CC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #1216831
DOI: 10.1039/C8SC04228D
CC(C)C[C@H](C(N)=O)N(CC1CCN(C(=O)OC(C)(C)C)CC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #1681387
solid
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](C(N)=O)N(CC1CCNCC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #1681388
solid
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(CN([C@@H]2CC(F)(F)CCNC2=O)S(=O)(=O)c2ccc(Cl)cc2)CC1
Reaction #1870586
4-{[(4-chloro-benzenesulfonyl)-((R)-5,5-difluoro-2-oxo-azepan-3-yl)-amino]-methyl}-piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCCC(F)(F)C[C@H]1N(CC1CCNCC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #1870587
4-chloro-N-((R)-5,5-difluoro-2-oxo-azepan-3-yl)-N-piperidin-4-ylmethyl-benzenesulfonamide
Rendement 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](C(N)=O)N(CC1CCN(C(=O)OC(C)(C)C)CC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #1981021
solid
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](C(N)=O)N(CC1CCNCC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #1981022
solid
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCCC(F)(F)CC1N(CC1CCNCC1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #2409198
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(CN(C2CC(F)(F)CCNC2=O)S(=O)(=O)c2ccc(Cl)cc2)CC1
Reaction #2418446
DOI: 10.1039/C8SC04228D