2-Methoxybenzylamine → HCID 44223905, compound

HRID 1803085Notes

Reaction equation

HRID 1803085 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-])=O)[CH:8]=2)[N:3]=1.[CH3:15][O:16][C:17]1[CH:24]=[CH:23][CH:22]=[CH:21][C:18]=1[CH2:19][NH2:20].[CH3:25][N:26]1[CH2:31][CH2:30][N:29]([CH2:32][C:33](O)=[O:34])[CH2:28][CH2:27]1>>[CH3:15][O:16][C:17]1[CH:24]=[CH:23][CH:22]=[CH:21][C:18]=1[CH2:19][NH:20][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH:12][C:33](=[O:34])[CH2:32][N:29]3[CH2:30][CH2:31][N:26]([CH3:25])[CH2:27][CH2:28]3)[CH:8]=2)[N:3]=1

Participants

4

Reactant 3

HCID 812922-MethoxybenzylamineHCID 2762732(4-Methylpiperazin-1-yl)acetic acidHCID 109217232-Chloro-6-nitroquinoline

Product 1

HCID 44223905HCID 44223905, compound

Procedure

The title compound, MS: m/e=420.0 (M+H+), was prepared in accordance with the general method of example 16 from 2-chloro-6-nitro-quinoline, 2-methoxy-benzylamine and 4-methyl-piperazin-1-yl acetic acid.

Sources & evidence

ORD record
ord-bdbc717196624d67a11c358afdb06281
Source dataset
uspto-grants-2013_01
Patent number
US08350028B2

Reaction notes

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