2-(Benzylamino)pyridine → HCID 21395228, compound

HRID 2398075

Reaction equation

HRID 2398075 reaction equation
Cl[CH2:2][CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][CH:8]([NH:11][C:12](=[O:20])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[CH3:19])[CH2:7][CH2:6]1.[CH2:21]([NH:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][N:30]=1)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>>[CH2:21]([N:28]([CH2:2][CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][CH:8]([NH:11][C:12](=[O:20])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[CH3:19])[CH2:7][CH2:6]1)[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][N:30]=1)[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1

Participants

3

Procedure

The title compound is prepared in a similar manner to Example 11 from 1-(3-chloropropyl)-4-(2-methylbenzamido)piperidine and 2-(benzylamino)pyridine.

Sources & evidence

ORD record
ord-6564bb3ad6ca4fff9124637d894a74fd
Source dataset
uspto-grants-1977_05
Patent number
US04024147

Linked notes

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