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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 499142생성일: 2026년 10월 25일

Hydrochloric Acid → 6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXYLIC Acid

https://huagongshe.com/reaction/499142

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물6-[4-(2-Trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid methyl esterHCID 66849526—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXYLIC AcidHCID 4548737095%

반응 단계

To a solution of 6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid methyl ester (4.436 g, 11.25 mmol) in tetrahydrofuran (50 mL) and water (25 mL) was added lithium hydroxide monohydrate (2.30 g, 54.81 mmol). The reaction mixture was stirred at ambient temperature for 23 h and the pH of the solution was adjusted to ˜3 with concentrated hydrochloric acid (5.3 mL) at 0° C. The mixture was concentrated. Ethyl acetate (100 mL) was added to the residue and the product was precipitated. The solid was collected by filtration, washed with ethyl acetate and dried in vacuo to afford the title compound (3.60 g). The aqueous layer was extracted with ethyl acetate, dried over Na2SO4 and concentrated to give the second portion of title compound (0.463 g). The total amount of product was 4.063 g (95% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767677B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-b33c8f5d7f594556a249c53d7e98c5ab
출처 메모uspto-grants-2010_08