2-Methoxybenzylamine → HCID 86634415, compound

HRID 1803068Notes

Reaction equation

HRID 1803068 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][CH2:25][N:26]1[CH2:31][CH2:30][O:29][CH2:28][CH2:27]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][CH2:25][N:26]3[CH2:31][CH2:30][O:29][CH2:28][CH2:27]3)[CH:8]=2)[N:3]=1

Participants

4

Reactant 3

HCID 812922-MethoxybenzylamineHCID 4082852-MorpholinoethylamineHCID 6075022,6-Dichloroquinoline

Product 1

HCID 86634415HCID 86634415, compound

Procedure

The title compound, MS: m/e=393.4 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 2-methoxybenzylamine and N-(2-aminoethyl)morpholine.

Sources & evidence

ORD record
ord-d909a50f0dd04969813c594fc03a9ad1
Source dataset
uspto-grants-2013_01
Patent number
US08350028B2

Reaction notes

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