4-Phenylpiperidine → 4-Phenyl-1-piperidinepropanamine, hydrochloride
Reaction equation
[C:1]1([CH:7]2[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:13][CH:14]([CH3:17])[C:15]#[N:16]>>[ClH:13].[C:1]1([CH:7]2[CH2:8][CH2:9][N:10]([CH2:17][CH2:14][CH2:15][NH2:16])[CH2:11][CH2:12]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
The above compound is prepared as described in Example 1A and B except that 4-phenylpiperidine is employed in place of 4-phenyl-1,2,3,6-tetrahydropyridine and chloropropionitrile is used in place of 4-bromobutyronitrile.
Workup
- customThe above compound is prepared
Sources & evidence
- ORD record
- ord-b6b97fb041cb437085afaba4dd6e4313
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03995045
Reaction notes
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