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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68458생성일: 2026년 10월 25일

Sodium hydride → 6-Chloro-2-methyl-4-({5-[(morpholin-4-yl)carbonyl]pyridin-2-yl}amino)-2,3-dihydropyridazin-3-one

https://huagongshe.com/reaction/68458

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참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4,6-Dichloro-2-methylpyridazin-3(2H)-oneHCID 12409910—
반응물(6-Aminopyridin-3-yl)(morpholino)methanoneHCID 59259223—
용매DimethylformamideHCID 6228—
생성물6-Chloro-2-methyl-4-({5-[(morpholin-4-yl)carbonyl]pyridin-2-yl}amino)-2,3-dihydropyridazin-3-oneHCID 5766277829.6%

반응 조건

온도0 °C

반응 단계

(6-Amino-pyridin-3-yl)-morpholin-4-yl-methanone (2.921 g, 14.11 mmol) was suspended in 50 mL dimethylformamide and cooled to 0° C. Sodium hydride 60% suspension in mineral oil (847 mg, 21.2 mmol) was added. This was stirred at room temperature for 30 minutes and was cooled to 0° C. 4,6-Dichloro-2-methyl-2H-pyridazin-3-one (1.256 g, 7.056 mmol) was added. After 2 hours, this was partitioned between saturated aqueous ammonium chloride solution and ethylacetate. The ethylacetate layer was dried over anhydrous MgSO4, concentrated in vacuo, and purified by flash chromatography (2% MeOH/CH2Cl2) to yield 6-Chloro-2-methyl-4-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-2H-pyridazin-3-one (732 mg, 2.09 mmol). MS (ESI) 350.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822457B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d7787870a04e4dc69a0b1ea4986de9a4
출처 메모uspto-grants-2014_09