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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6911생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/6911

반응식

참여 물질

역할이름HCID투입량
반응물ButyrohydrazideHCID 77079—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-(Pyrimidin-2-yl)piperidine-4-carboxylic acidHCID 2767267—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매DichloromethaneHCID 6344—
용매Sodium BicarbonateHCID 516892—
생성물1-Pyrimidin-2-yl-piperidine-4-carboxylic acid N'-butyryl-hydrazideHCID 2354406962%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084145B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-4e299013dbfd48c1bf2a6e7afd13ee69
출처 메모uspto-grants-2006_08