2-Methoxybenzylamine → HCID 68435215, compound

HRID 1170078Notes

Reaction equation

HRID 1170078 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][O:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17][NH2:18].[CH3:23][NH:24][CH2:25][C:26]1[CH:27]=[N:28][CH:29]=[CH:30][CH:31]=1>>[CH3:13][O:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17][NH:18][C:6]1[CH:5]=[CH:4][C:3]2[C:2]([N:24]([CH3:23])[CH2:25][C:26]3[CH:27]=[N:28][CH:29]=[CH:30][CH:31]=3)=[CH:11][CH:10]=[CH:9][C:8]=2[N:7]=1

Participants

4

Reactant 3

HCID 812922-MethoxybenzylamineHCID 883933-(Methylaminomethyl)pyridineHCID 142210335-Bromo-2-chloroquinoline

Product 1

HCID 68435215HCID 68435215, compound

Procedure

The title compound, MS: m/e=385.0 (M+H+), was prepared in accordance with the general method of example 1 from 5-bromo-2-chloroquinoline, 2-methoxybenzylamine and N-methyl-3-picolylamine.

Sources & evidence

ORD record
ord-a732737a0ae04979a1f888fede1ca42d
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Reaction notes

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