2-Chloro-5-nitroquinoline → HCID 178425482, compound

HRID 1170160

Reaction equation

HRID 1170160 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:20][C:19]([CH2:21][NH2:22])=[CH:18][CH:17]=1.[NH:23]1[C:27]2[CH:28]=[CH:29][C:30]([CH:32]=O)=[CH:31][C:26]=2[N:25]=[CH:24]1>>[NH:23]1[C:27]2[CH:28]=[CH:29][C:30]([CH2:32][NH:1][C:4]3[C:5]4[CH:6]=[CH:7][C:8]([NH:22][CH2:21][C:19]5[O:20][C:16]([CH3:15])=[CH:17][CH:18]=5)=[N:9][C:10]=4[CH:11]=[CH:12][CH:13]=3)=[CH:31][C:26]=2[N:25]=[CH:24]1

Participants

4

Reactant 3

HCID 3192512-Chloro-5-nitroquinolineHCID 27246835-Methyl-2-furylmethylamineHCID 178418743HCID 178418743, compound

Product 1

HCID 178425482HCID 178425482, compound

Procedure

The title compound, MS: m/e=384.1 (M+H+), was prepared from 5-nitro-2-chloroquinoline, 5-methyl-2-furanmethanamine and 1H-benzimidazole-5-carbaldehyde as described in example 26.

Sources & evidence

ORD record
ord-ce3f18d5de2340cf986ed91da7b097b9
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Linked notes

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