2-Chloro-5-nitroquinoline → HCID 44217991, compound

HRID 1669708Notes

Reaction equation

HRID 1669708 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[CH3:15][C:16]1[O:17][C:18]2[C:24]([NH2:25])=[CH:23][CH:22]=[CH:21][C:19]=2[CH:20]=1>>[CH3:15][C:16]1[O:17][C:18]2[C:24]([NH:25][C:8]3[CH:7]=[CH:6][C:5]4[C:4]([NH2:1])=[CH:13][CH:12]=[CH:11][C:10]=4[N:9]=3)=[CH:23][CH:22]=[CH:21][C:19]=2[CH:20]=1

Participants

3

Reactant 2

HCID 3192512-Chloro-5-nitroquinolineHCID 31574852-Methyl-benzofuran-7-ylamine

Product 1

HCID 44217991HCID 44217991, compound

Procedure

The title compound, MS: m/e=290.3 (M+H+), was prepared in accordance with the general method of example 1 from 5-nitro-2-chloroquinoline and (2-methyl-1-benzofuran-7-yl)amine.

Sources & evidence

ORD record
ord-49d01796406a4aaea664da7dd0fa9c4d
Source dataset
uspto-grants-2011_08
Patent number
US07989628B2

Reaction notes

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