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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 592180생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → (6-chloro-5-methylpyridin-3-yl)-N-(5-(pyridazin-3-yl)pyridin-2-yl)acetamide

https://huagongshe.com/reaction/592180

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2-(6-Chloro-5-methylpyridin-3-yl)acetic acidHCID 55267357—
반응물5-(Pyridazin-3-yl)pyridin-2-amineHCID 58447663—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
생성물(6-chloro-5-methylpyridin-3-yl)-N-(5-(pyridazin-3-yl)pyridin-2-yl)acetamideHCID 86657954—

반응 단계

A mixture of 2-(6-chloro-5-methylpyridin-3-yl)acetic acid 86-7 (241 mg, 1.3 mmol), 5-(pyridazin-3-yl)pyridin-2-amine 145-3 (224 mg, 1.3 mmol), 1,3-dicyclohexylcarbodiimide (325 mg, 1.6 mmol) and 4-(dimethylamino)pyridine (26 mg, 0.26 mmol) in DMF (6 mL) was stirred at room temperature for 10 hours. The reaction mixture was filtered to remove the solid and the filtrate was diluted with ethyl acetate, washed with water and brine, dried over Na2SO4 and concentrated to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, eluted with 5% methanol in dichloromethane to give 2-((6-chloro-5-methylpyridin-3-yl)-N-(5-(pyridazin-3-yl)pyridin-2-yl)acetamide 145-4 as pale yellow solid. MS m/z 340.2 (M+1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09238646B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-6e61d1d256ec4951bebcd85450e3002c
출처 메모uspto-grants-2016_01