4-(4-Fluorophenyl)piperidine → HCID 15390679, compound
Reaction equation
CS(O[CH2:6][CH2:7][CH2:8][CH:9]1[C:13]2[CH:14]=[C:15]([F:18])[CH:16]=[CH:17][C:12]=2[O:11][CH2:10]1)(=O)=O.[F:19][C:20]1[CH:25]=[CH:24][C:23]([CH:26]2[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]2)=[CH:22][CH:21]=1>>[F:18][C:15]1[CH:16]=[CH:17][C:12]2[O:11][CH2:10][CH:9]([CH2:8][CH2:7][CH2:6][N:29]3[CH2:30][CH2:31][CH:26]([C:23]4[CH:22]=[CH:21][C:20]([F:19])=[CH:25][CH:24]=4)[CH2:27][CH2:28]3)[C:13]=2[CH:14]=1Participants
3
Procedure
The title compound, 11a, was prepared from 3-(2,3-dihydro-5-fluoro-benzofuran-3-yl)-1-propyl methanesulfonate (4.2 g) and 4-(4-fluorophenyl)piperidine (5.5 g) by the method described in EXAMPLE 2. Yield: 1.8 g, mp: 83-85° C.
Sources & evidence
- ORD record
- ord-8474cd5d63d443359d856740e30c5945
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06207677B1
Reaction notes
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