4-Benzylpiperidine → HCID 15101078, compound

HRID 1088766Notes

Reaction equation

HRID 1088766 reaction equation
[CH2:1]([CH:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[CH2:15][C:16]([N:18]1[CH2:23][CH:22]=[C:21]([C:24]2[CH:29]=[C:28]([Cl:30])[CH:27]=[CH:26][C:25]=2[Cl:31])[N:20]2[N:32]=[CH:33][C:34]([C:35]#[N:36])=[C:19]12)=[O:17]>>[Cl:31][C:25]1[CH:26]=[CH:27][C:28]([Cl:30])=[CH:29][C:24]=1[C:21]1[N:20]2[N:32]=[CH:33][C:34]([C:35]#[N:36])=[C:19]2[N:18]([C:16](=[O:17])[CH2:15][N:11]2[CH2:12][CH2:13][CH:8]([CH2:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH2:9][CH2:10]2)[CH2:23][CH:22]=1

Participants

3

Procedure

The above compound was prepared by the reaction of 4-benzylpiperidine with the compound of Example 9 by the procedure of Example 16, mp 157°-158° C.

Sources & evidence

ORD record
ord-79173088566745bb90d47042a7f5ead3
Source dataset
uspto-grants-1990_10
Patent number
US04963553

Reaction notes

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