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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622613Generated: October 30, 2026

2-Aminonicotinic acid → 3-Pyridinecarboxylic acid, 2-amino-, 2-[4-(1-methylethyl)benzoyl]hydrazide

https://huagongshe.com/reaction/1622613

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminonicotinic acidHCID 72930—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-isopropylbenzohydrazideHCID 219400—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-Pyridinecarboxylic acid, 2-amino-, 2-[4-(1-methylethyl)benzoyl]hydrazideHCID 6674853366.7%

Reaction Steps

A mixture of 4-(1-methylethyl)benzohydrazide (2194 mg), HOBt.H2O (2073 mg), EDCI HCl (2595 mg) and 2-aminopyridine-3-carboxylic acid (1700 mg) in dehydrated DMF (50 mL) was stirred at 60° C. overnight. The reaction mixture was added to a saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was crystallized from a mixture of ethyl acetate and diisopropyl ether to give the title compound (2.4489 g) as a white solid. The mother liquor was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (276.1 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778934B2
Source datasetuspto-grants-2014_07
ORD IDord-ee5a42176e6a49f5949e149c37c54ebf
Source noteuspto-grants-2014_07