Substructure Search

1362995

O=C1CCN(S(=O)(=O)c2ccc(CNC(=O)c3ccc(Cl)cc3)cc2)CC1
Reaction #233794
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(S(=O)(=O)N2CCC3(CC2)OCCO3)cc1)c1ccc(Cl)cc1
Reaction #1310833
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(S(=O)(=O)N2CCC3(CC2)OCCO3)cc1)c1ccc(Cl)cc1
Reaction #1764997
sulfonamide 4-chloro-N-[4-(1,4-dioxa-8-azaspiro[4.5]dec-8-ylsulfonyl)benzyl]benzamide
Yield 59.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(S(=O)(=O)c2ccc(CNC(=O)c3ccc(Cl)cc3)cc2)CC1
Reaction #1764998
ketone 4-chloro-N-{4-[(4-oxo-1-piperidinyl)sulfonyl]benzyl}benzamide
Yield 82.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(S(=O)(=O)N2CCC3(CC2)OCCO3)cc1)c1ccc(Cl)cc1
Reaction #2307337
sulfonamide 4-chloro-N-[4-(1,4-dioxa-8-azaspiro[4.5]dec-8-ylsulfonyl)benzyl]benzamide
Yield 59.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(S(=O)(=O)c2ccc(CNC(=O)c3ccc(Cl)cc3)cc2)CC1
Reaction #2307338
ketone 4-chloro-N-{4-[(4-oxo-1-piperidinyl)sulfonyl]benzyl}benzamide
Yield 82.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(S(=O)(=O)c2ccc(CNC(=O)c3ccc(Cl)cc3)cc2)CC1
Reaction #2422176
DOI: 10.1039/C8SC04228D