2-Phenoxyethanamine → HCID 25235527, compound

HRID 1948999Notes

Reaction equation

HRID 1948999 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.[O:13]([CH2:20][CH2:21][NH2:22])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[CH3:23][O:24][C:25]1[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=1)[CH2:28][NH2:29]>>[CH3:23][O:24][C:25]1[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=1)[CH2:28][NH:29][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:22][CH2:21][CH2:20][O:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH:11]=[CH:10]2

Participants

4

Reactant 3

HCID 156512-PhenoxyethanamineHCID 211563-MethoxybenzylamineHCID 6075022,6-Dichloroquinoline

Product 1

HCID 25235527HCID 25235527, 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, 2-phenoxyethylamine and 3-methoxybenzylamine.

Sources & evidence

ORD record
ord-44fa475342e941c6adcf79caf203b830
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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