4-Fluorobenzenesulfonyl chloride → HCID 23288138, compound
Reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[C:19]3[C:14](=[CH:15][CH:16]=[C:17]([Cl:20])[CH:18]=3)[C:13]([CH:21]3[CH2:26][CH2:25][N:24]([CH3:27])[CH2:23][CH2:22]3)=[CH:12]2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.ClC1C=C2C(C(C3CCN(C)CC3)=CN2)=CC=1.FC1C=CC(S(Cl)(=O)=O)=CC=1>>[Cl:20][C:17]1[CH:18]=[C:19]2[C:14]([C:13]([CH:21]3[CH2:26][CH2:25][N:24]([CH3:27])[CH2:23][CH2:22]3)=[CH:12][N:11]2[S:8]([C:5]2[CH:6]=[CH:7][CH:2]=[CH:3][CH:4]=2)(=[O:10])=[O:9])=[CH:15][CH:16]=1Participants
4
Procedure
1-(4-Fluorophenylsulfonyl)-6-chloro-3-(1-methyl-4-piperidinyl)indole: (26.8 mg, 65%), from 6-chloro-3-(1-methyl-4-piperidinyl)-1H-indole (Example 5b, 25 mg, 0.10 mmol) and 4-fluorophenylsulfonyl chloride (29.2 mg, 0.15 mmol), HRMS-FAB+ for C20H20N2O2SClF, calculated MH+ : 407.09964; found: 407.09929.
Sources & evidence
- ORD record
- ord-1636e22e03a84594b4c2f8a961763e76
- Source dataset
- uspto-grants-2000_10
- Patent number
- US06133287
Reaction notes
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