Substructure Search

1276804

O=C1CCN(S(=O)(=O)c2ccc(CNC(=O)c3ccc(Cl)cc3)cc2)CC1
Reaction #233794
DOI: 10.1039/C8SC04228D
CCCCCCNC1CCN(S(=O)(=O)c2ccc(CNC(=O)c3ccc(Cl)cc3)cc2)CC1
Reaction #1021023
DOI: 10.1039/C8SC04228D
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
—
Reaction #1764999
powder
Yield 36.0%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
—
Reaction #2307339
powder
Yield 36.0%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