N-(3-Aminopropyl)morpholine → HCID 86634416, compound

HRID 1803069Notes

Reaction equation

HRID 1803069 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][CH2:26][N:27]1[CH2:32][CH2:31][O:30][CH2:29][CH2:28]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][CH2:26][N:27]3[CH2:32][CH2:31][O:30][CH2:29][CH2:28]3)[CH:8]=2)[N:3]=1

Participants

4

Reactant 3

HCID 61055N-(3-Aminopropyl)morpholineHCID 812922-MethoxybenzylamineHCID 6075022,6-Dichloroquinoline

Product 1

HCID 86634416HCID 86634416, compound

Procedure

The title compound, MS: m/e=407.5 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 2-methoxybenzylamine and 4-(3-aminopropyl)morpholine.

Sources & evidence

ORD record
ord-e77c42f2b58c4332b7c68c7c5b16d8c0
Source dataset
uspto-grants-2013_01
Patent number
US08350028B2

Reaction notes

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