Pyrrolidine → 2-Aminomethyl-4-(1,1-dimethylethyl)-6-(1-pyrrolidinylsulfonyl)-phenol hydrochloride
Reaction equation
C([NH:4][CH2:5][C:6]1[CH:11]=[C:10]([C:12]([CH3:15])([CH3:14])[CH3:13])[CH:9]=[C:8]([S:16]([Cl:19])(=[O:18])=[O:17])[C:7]=1[OH:20])(=O)C.[NH:21]1[CH2:25][CH2:24][CH2:23][CH2:22]1>>[ClH:19].[NH2:4][CH2:5][C:6]1[CH:11]=[C:10]([C:12]([CH3:13])([CH3:14])[CH3:15])[CH:9]=[C:8]([S:16]([N:21]2[CH2:25][CH2:24][CH2:23][CH2:22]2)(=[O:17])=[O:18])[C:7]=1[OH:20]Participants
3
Procedure
This compound is prepared analogously to Examples 11 c and 11 d from 2-acetamidomethyl-6-chlorosulfonyl-4-(1,1-dimethylethyl)-phenol and pyrrolidine.
Sources & evidence
- ORD record
- ord-8a24a87a7e6747d8b7da6b9b3d65e1b0
- Source dataset
- uspto-grants-1988_08
- Patent number
- US04766241
Reaction notes
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