2-Methoxybenzylamine → HCID 24987485, compound

HRID 1170083Notes

Reaction equation

HRID 1170083 reaction equation
Br[C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](Cl)=[N:7]2.[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:30]=[CH:29][CH:28]=[CH:27][C:24]=1[CH2:25][NH2:26]>>[CH3:21][O:22][C:23]1[CH:30]=[CH:29][CH:28]=[CH:27][C:24]=1[CH2:25][NH:26][C:2]1[C:3]2[CH:4]=[CH:5][C:6]([NH:20][CH2:19][C:17]3[O:18][C:14]([CH3:13])=[CH:15][CH:16]=3)=[N:7][C:8]=2[CH:9]=[CH:10][CH:11]=1

Participants

4

Reactant 3

HCID 812922-MethoxybenzylamineHCID 27246835-Methyl-2-furylmethylamineHCID 142210335-Bromo-2-chloroquinoline

Product 1

HCID 24987485HCID 24987485, compound

Procedure

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

Sources & evidence

ORD record
ord-ef2f6826dbe144e0a27bb35335e3eeb1
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Reaction notes

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