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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 386569생성일: 2026년 10월 26일

Hydrochloric Acid → 1-(4-cyano-3-fluorophenyl)-6-oxo-4-(piperidin-4-yloxy)-1,6-dihydropyridazine-3-carbonitrile HCl salt

https://huagongshe.com/reaction/386569

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl EtherHCID 3283—
반응물1,4-DioxaneHCID 31275—
반응물tert-Butyl 4-(3-carbamoyl-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazin-4-yloxy)piperidine-1-carboxylateHCID 67445416—
용매DichloromethaneHCID 6344—
생성물1-(4-cyano-3-fluorophenyl)-6-oxo-4-(piperidin-4-yloxy)-1,6-dihydropyridazine-3-carbonitrile HCl saltHCID 67447026100%

반응 단계

To a stirring solution of tert-butyl 4-(3-cyano-1-(4-cyano-3-fluorophenyl)-6-oxo-1,6-dihydropyridazin-4-yloxy)piperidine-1-carboxylate (example 34) (22 mg, 0.050 mmol) in DCM (3 mL) at room temperature under argon was added 4 M HCl in dioxane (0.375 mL, 1.5 mmol). The reaction mixture was stirred at room temperature overnight. Et2O (10 mL) was added to the reaction mixture. The solid product was collected by filtration and further washed with ether (2 mL×2). After drying under vacuum for 2 hours, 19 mg (100%) of 1-(4-cyano-3-fluorophenyl)-6-oxo-4-(piperidin-4-yloxy)-1,6-dihydropyridazine-3-carbonitrile HCl salt was obtained as an off-white solid. MS (ESI) 340 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372837B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-736e5b60b2b9431eb66248be4cd7047a
출처 메모uspto-grants-2013_02