4-Nitrobenzoic Acid → HCID 86701930, compound

HRID 717916Notes

Reaction equation

CC(C)CC[NH2:5].[N:7]1[CH:8]=[CH:9][N:10]2[CH:15]=[C:14]([C:16]([OH:18])=O)[CH:13]=[CH:12][C:11]=12.[N+:19]([C:22]1[CH:30]=[CH:29][C:25]([C:26](O)=O)=[CH:24][CH:23]=1)([O-:21])=[O:20]>>[N+:19]([C:22]1[CH:30]=[CH:29][C:25]([CH2:26][NH:5][C:16]([C:14]2[CH:13]=[CH:12][C:11]3[N:10]([CH:9]=[CH:8][N:7]=3)[CH:15]=2)=[O:18])=[CH:24][CH:23]=1)([O-:21])=[O:20]

Participants

Reactant 3

HCID 61084-Nitrobenzoic Acid

HCID 7894Isoamylamine

HCID 7075376Imidazo(1,2-a)pyridine-6-carboxylic acid

Product 1

HCID 86701930HCID 86701930, compound

Procedure

The title compound was prepared as described in Example 1A, substituting (4-nitrophenyl)methanamine for 3-methylbutan-1-amine and imidazo[1,2-a]pyridine-6-carboxylic acid for 4-nitrobenzoic acid.

Sources & evidence

ORD record: ord-18c9899ee940482887c39ffbb893948c
Source dataset: uspto-grants-2015_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09193723B2

Reaction notes

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