Methyl iodide → HCID 69663086, compound
Reaction equation
[C:1]1([S:7]([CH:10]([CH3:25])[CH:11]([CH3:24])[CH2:12][CH2:13][N:14]2[CH2:19][CH2:18][CH:17]([C:20]([F:23])([F:22])[F:21])[CH2:16][CH2:15]2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:26]I>>[C:1]1([S:7]([C:10]([CH3:26])([CH3:25])[CH:11]([CH3:24])[CH2:12][CH2:13][N:14]2[CH2:15][CH2:16][CH:17]([C:20]([F:23])([F:22])[F:21])[CH2:18][CH2:19]2)(=[O:9])=[O:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
Prepared from 1-(4-benzenesulfonyl-3-methylpentyl)-4-trifluoromethylpiperidine (example 126) and methyl iodide by the method of Example 187.
Sources & evidence
- ORD record
- ord-d5a18514ea554d1bacd839196cdf7ff5
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07101892B2
Reaction notes
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