2-Phenoxyethanamine → HCID 68574339, compound

HRID 1948996Notes

Reaction equation

HRID 1948996 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.[NH2:23][CH2:24][C:25]1[CH:30]=[CH:29][N:28]=[CH:27][CH:26]=1>>[O:13]([CH2:20][CH2:21][NH:22][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH:23][CH2:24][C:25]3[CH:30]=[CH:29][N:28]=[CH:27][CH:26]=3)[CH:8]=2)[N:3]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

4

Reactant 3

HCID 156512-PhenoxyethanamineHCID 773174-PyridinemethanamineHCID 6075022,6-Dichloroquinoline

Product 1

HCID 68574339HCID 68574339, compound

Procedure

The title compound, MS: m/e=371.1 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 2-phenoxyethylamine and 4-(aminomethyl)pyridine.

Sources & evidence

ORD record
ord-aa94b810ab634c9881156caca4fc8c37
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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