Reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][C:5](=[CH2:8])[CH2:4][CH2:3]1.N1(CCC[C:18]2[CH:19]=[C:20]([NH:28][C:29](=[O:31])[CH3:30])[CH:21]=[C:22]([C:24]([F:27])([F:26])[F:25])[CH:23]=2)CCCCC1>>[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([CH2:8][C:18]2[CH:19]=[C:20]([NH:28][C:29](=[O:31])[CH3:30])[CH:21]=[C:22]([C:24]([F:25])([F:26])[F:27])[CH:23]=2)[CH2:4][CH2:3]1Participants
3
Procedure
N-[3-(1-Methyl-piperidin-4-ylmethyl)-5-trifluoromethyl-phenyl]-acetamide was prepared from 1-Methyl-4-methylene-piperidine similar to that described in the preparation of N-[3-(3-piperidin-1-yl-propyl)-5-trifluoromethyl-phenyl]-acetamide.
Sources & evidence
- ORD record
- ord-6cba07ca4b0b40b99888a42cfdde22bf
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247556B2
Linked notes
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