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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2391422생성일: 2026년 10월 25일

Hydrochloric Acid → N-{5-[(2-{[(1-hydroxycyclopropyl)carbonyl]amino}imidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/2391422

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcetateHCID 8857—
반응물Sodium HydroxideHCID 14798—
반응물1-({[6-(3-{[(1,3-dimethyl-1H-pyrazol-5-yl)carbonyl]amino}-4-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]amino}carbonyl)cyclopropyl acetateHCID 57505660—
용매TetrahydrofuranHCID 8028—
생성물N-{5-[(2-{[(1-hydroxycyclopropyl)carbonyl]amino}imidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 5750566186%

반응 단계

To a solution of 1-({[6-(3-{[(1,3-dimethyl-1H-pyrazol-5-yl)carbonyl]amino}-4-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]amino}carbonyl)cyclopropyl acetate (130 mg, 0.25 mmol) in tetrahydrofuran (2 mL) was added 1N aqueous sodium hydroxide solution (2 mL), and the mixture was stirred at room temperature for 2 hr. 1N Hydrochloric acid (2.5 mL) and ethyl acetate were added to the reaction mixture, and the aqueous layer was extracted with ethyl acetate (×3). Combined organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtrated. The filtrate was concentrated under reduced pressure, and the residue was washed with ethyl acetate/hexane to give the title compound (99 mg, 86%) as a pale-yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08273741B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-93bcb31157324996b5848f90983f208e
출처 메모uspto-grants-2012_09