4-Chlorobenzenesulfonyl chloride → 4-Chloro-1-{[2-(4-fluorophenyl)pyrrolidinyl]sulfonyl}benzene
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:12][CH2:11][CH2:10][NH:9]2)=[CH:4][CH:3]=1.[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([S:20](Cl)(=[O:22])=[O:21])=[CH:16][CH:15]=1>>[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([S:20]([N:9]2[CH2:10][CH2:11][CH2:12][CH:8]2[C:5]2[CH:4]=[CH:3][C:2]([F:1])=[CH:7][CH:6]=2)(=[O:22])=[O:21])=[CH:16][CH:15]=1Participants
3
Procedure
The title compound, white solid, m.p. 118° C. and MS: m/e=339 (M+) was prepared in accordance with the general method of example 1e from (RS)-2-(4-fluoro-phenyl)-pyrrolidine and 4-chloro-benzenesulfonyl chloride.
Sources & evidence
- ORD record
- ord-f0ef244431d64b329b69651aa450fc73
- Source dataset
- uspto-grants-2001_09
- Patent number
- US06284785B1
Reaction notes
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