2-Pyridinemethanamine → HCID 58450753, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]([Cl:13])=[CH:10][C:11]=1Cl)=[O:5])[CH3:2].[NH2:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=1>>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]([Cl:13])=[CH:10][C:11]=1[NH:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=1)=[O:5])[CH3:2]Participants
3
Procedure
From 4,6-dichloropyridine-3-carboxylic acid ethyl ester synthesized according to the method described in US2006/0217417 and 2-(aminomethyl)pyridine in a manner similar to Example 339, the title compound was obtained as a colorless crystalline powder (yield 71%).
Sources & evidence
- ORD record
- ord-4377e18544924b239cfd935882a475c0
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08575153B2
Reaction notes
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