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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943460생성일: 2026년 10월 27일

Acetyl chloride → 8-(6-acetamido-4-chloropyridin-2-ylamino)-6-chloro-N-(3-fluoropyridin-4-yl)imidazo[1,2-b]pyridazine-3-carboxamide

https://huagongshe.com/reaction/1943460

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물4-Chloropyridine-2,6-diamineHCID 237847—
반응물8-Bromo-6-chloro-N-(3-fluoropyridin-4-yl)imidazo[1,2-b]pyridazine-3-carboxamideHCID 59624495—
촉매DiisopropylethylamineHCID 81531—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물8-(6-acetamido-4-chloropyridin-2-ylamino)-6-chloro-N-(3-fluoropyridin-4-yl)imidazo[1,2-b]pyridazine-3-carboxamideHCID 5962461268.4%

반응 단계

To a solution of 4-chloropyridine-2,6-diamine (35.2 mg, 0.245 mmol) in THF (0.5 mL) was added 60% NaH (12.26 mg, 0.307 mmol). The mixture was stirred for 10 min. 5A (40 mg, 0.123 mmol) was added, followed by DMF (0.5 mL). The mixture was stirred at room temperature overnight. To the reaction mixture was added acetyl chloride (0.052 mL, 0.736 mmol) and a few drops of DIEA. The mixture was stirred at 65° C. for 20 min and then cooled to room temperature. Saturated NH4Cl was added and the resulting precipitate was collected by filtration, washed with water, and dried in vacuum to give crude 41A as a yellow solid (40 mg, 49%). HPLC Rt=3.283 min. (Chromolith SpeedROD 4.6×50 mm, 10-90% aqueous methanol containing 0.1% TFA, 4 min gradient, monitored at 220 nm), [M+H]=475.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08389527B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-165dcce456f54738aca5fe8e8331f26c
출처 메모uspto-grants-2013_03