3-Methoxybenzylamine → HCID 25235571, compound

HRID 1949018Notes

Reaction equation

HRID 1949018 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][C:14]1[O:18][C:17]([CH2:19][NH2:20])=[CH:16][CH:15]=1.[CH3:21][O:22][C:23]1[CH:24]=[C:25]([CH:28]=[CH:29][CH:30]=1)[CH2:26][NH2:27]>>[CH3:21][O:22][C:23]1[CH:24]=[C:25]([CH:28]=[CH:29][CH:30]=1)[CH2:26][NH:27][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:20][CH2:19][C:17]1[O:18][C:14]([CH3:13])=[CH:15][CH:16]=1)[CH:11]=[CH:10]2

Participants

4

Reactant 3

HCID 211563-MethoxybenzylamineHCID 6075022,6-DichloroquinolineHCID 27246835-Methyl-2-furylmethylamine

Product 1

HCID 25235571HCID 25235571, compound

Procedure

The title compound, MS: m/e=374.3 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 5-methyl-2-furanmethanamine and 3-methoxybenzylamine.

Sources & evidence

ORD record
ord-9055e960dba7460c91d4ec1a96fdfbbc
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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