3-Pyridinemethanamine → HCID 25235489, compound

HRID 1948995Notes

Reaction equation

HRID 1948995 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7](Cl)[CH:8]=2)[N:3]=1.[CH3:13][O:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17][NH2:18].[NH2:23][CH2:24][C:25]1[CH:26]=[N:27][CH:28]=[CH:29][CH:30]=1>>[CH3:13][O:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17][NH:18][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH:23][CH2:24][C:25]3[CH:26]=[N:27][CH:28]=[CH:29][CH:30]=3)[CH:8]=2)[N:3]=1

Participants

4

Reactant 3

HCID 310183-PyridinemethanamineHCID 812922-MethoxybenzylamineHCID 6075022,6-Dichloroquinoline

Product 1

HCID 25235489HCID 25235489, compound

Procedure

The title compound, MS: m/e=371.0 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 2-methoxybenzylamine and 3-(aminomethyl)pyridine.

Sources & evidence

ORD record
ord-1716cb45aeca4631b9dc325d6446f9ba
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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