2-Methoxybenzylamine → HCID 68574337, compound

HRID 1949043Notes

Reaction equation

HRID 1949043 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].[CH3:23][O:24][CH2:25][CH2:26][O:27][C:28]1[CH:29]=[C:30]([CH:33]=[CH:34][CH:35]=1)[C:31]#[N:32]>>[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:32][CH2:31][C:30]3[CH:33]=[CH:34][CH:35]=[C:28]([O:27][CH2:26][CH2:25][O:24][CH3:23])[CH:29]=3)[CH:8]=2)[N:3]=1

Participants

4

Reactant 3

HCID 812922-MethoxybenzylamineHCID 6075022,6-DichloroquinolineHCID 247116333-(2-Methoxyethoxy)benzonitrile

Product 1

HCID 68574337HCID 68574337, compound

Procedure

The title compound, MS: m/e=444.4 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 2-methoxybenzylamine and 3-(2-methoxy-ethoxy)-benzonitrile (CAS 80407-67-6).

Sources & evidence

ORD record
ord-f801eddcd2b243f7b92898f6a5f52e76
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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