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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6911Generated: October 26, 2026

Butyrohydrazide → 1-Pyrimidin-2-yl-piperidine-4-carboxylic acid N'-butyryl-hydrazide

https://huagongshe.com/reaction/6911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyrohydrazideHCID 77079—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-(Pyrimidin-2-yl)piperidine-4-carboxylic acidHCID 2767267—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product1-Pyrimidin-2-yl-piperidine-4-carboxylic acid N'-butyryl-hydrazideHCID 2354406962%

Reaction Steps

A mixture of 1-pyrimidin-2-yl-piperidine-4-carboxylic acid (3.0 g, 14.5 mmol)(see reference U.S. Pat. No. 4,826,843), 1-hydroxybenzotriazole hydrate (1.96 g, 14.5 mmol) and 1-(3-dimethylaminopropyl-3-ethylcarbodiimide hydrochloride (2.78 g, 14.5 mmol) in dichloromethane (100 ml) was stirred for 10 minutes. Butyric acid hydrazide (1.78 g, 17.4 mmol) was added and the reaction mixture was stirred under a nitrogen atmosphere for 18 hours. The reaction mixture was diluted with dichloromethane (100 ml) and sodium hydrogen carbonate solution was added. The reaction mixture was concentrated under reduced pressure and the solid formed was isolated by filtration. The material obtained was dried under vacuum at 40° C. to give the title compound (2.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084145B2
Source datasetuspto-grants-2006_08
ORD IDord-4e299013dbfd48c1bf2a6e7afd13ee69
Source noteuspto-grants-2006_08