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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396919Generated: October 30, 2026

6-Aminonicotinic acid → 6-Aminonicotinamide

https://huagongshe.com/reaction/2396919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Aminonicotinic acidHCID 18496—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product6-AminonicotinamideHCID 9500162.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 6-aminopyridine-3-carboxylic acid (8.36 g), N-hydroxybenzotriazole (10.2 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (12.8 g) and 4-dimethylaminopyridine (8.12 g) in N,N-dimethylformamide (300 ml) was stirred at 0° C. for 15 minutes. (2E,4E)- and (2Z,4E)-4-methyl-2,4-heptadien-1-ylamine (7.7 g) was added to the mixture. The solution was stirred at 0° C. for 2 hours and then at room temperature overnight. The mixture was evaporated in vacuo and the residue was diluted with water. The resulting precipitate was filtered and washed with water to give N-[(2E,4E)- and (2Z-4E)-4-methyl-2,4-heptadien-1-yl]-6-amino-3-pyridinecarboxamide (13.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05495023
Source datasetuspto-grants-1996_02
ORD IDord-56a82611f4a1446f942a6b2b28f4ad44
Source noteuspto-grants-1996_02