Piperidine → 3-{2-[(2-Fluoro-phenyl)-piperidin-1-yl-methyl]-pyrrol-1-yl}-propionitrile
Reaction equation
[N:1]1([CH2:6][CH2:7][C:8]#[N:9])[CH:5]=[CH:4][CH:3]=[CH:2]1.[Cl-].[F:11][C:12]1[CH:24]=[CH:23][CH:22]=[CH:21][C:13]=1[CH:14]=[N+:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1.FC1C=CC=CC=1C=O.N1CCCCC1>>[F:11][C:12]1[CH:24]=[CH:23][CH:22]=[CH:21][C:13]=1[CH:14]([N:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1)[C:2]1[N:1]([CH2:6][CH2:7][C:8]#[N:9])[CH:5]=[CH:4][CH:3]=1Participants
5
Procedure
The preparation was carried out in accordance with general synthesis instructions 4 from 3-pyrrol-1-yl-propionitrile and 1-(2-fluoro-benzylidene)-piperidinium chloride, which had been prepared in accordance with example 3 from 2-fluorobenzaldehyde and piperidine.
Sources & evidence
- ORD record
- ord-7caf6ae5c4664fdda083e12347e3fb7b
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07034018B2
Reaction notes
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