Benzenesulfonyl chloride → HCID 71257509, compound
Reaction equation
[C:1]1([S:7](Cl)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:11]([N:18]1[CH2:23][CH2:22][CH:21]([CH2:24][NH2:25])[CH2:20][CH2:19]1)([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12]>>[C:14]([O:13][C:11]([N:18]1[CH2:23][CH2:22][CH:21]([CH2:24][NH:25][S:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)(=[O:9])=[O:8])[CH2:20][CH2:19]1)=[O:12])([CH3:17])([CH3:16])[CH3:15]Participants
3
Procedure
According to Reference Example 1, benzenesulfonylchloride and 1-Boc-4-(aminomethyl)piperidine were condensed to give the title compound.
Workup
- customcondensed
Sources & evidence
- ORD record
- ord-fef7debd1f2b4f2e9bdc82e5122a982e
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08772297B2
Reaction notes
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