2-Methoxybenzylamine → HCID 25235528, compound

HRID 1949006Notes

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]>>[CH3:13][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:18][CH2:17][C:16]3[CH:19]=[CH:20][CH:21]=[CH:22][C:15]=3[O:14][CH3:13])[CH:8]=2)[N:3]=1

Participants

Reactant 2

HCID 812922-Methoxybenzylamine

HCID 6075022,6-Dichloroquinoline

Product 1

HCID 25235528HCID 25235528, compound

Procedure

The title compound, MS: m/e=400.4 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline and 2-methoxybenzylamine.

Sources & evidence

ORD record: ord-8fc50ce44a9a457899ca97afe49fb307
Source dataset: uspto-grants-2013_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08399674B2

Reaction notes

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