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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64614생성일: 2026년 10월 24일

Oxalic Acid → 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(4-fluorophenyl)piperazine oxalate

https://huagongshe.com/ko/reaction/64614

반응식

참여 물질

역할이름HCID투입량
반응물Oxalic AcidHCID 971—
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물1-(4-Fluorophenyl)piperazineHCID 75260—
반응물3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazoleHCID 10910880—
용매DimethylformamideHCID 6228—
생성물1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(4-fluorophenyl)piperazine oxalateHCID 13520733—

반응 단계

A mixture of 5.0 g of 3-(3-chloropropyl)-6-fluoro-1,2-benzisoxazole, 4.0 g of 1-(4-fluorophenyl)piperazine, 10 g of potassium carbonate and a few crystals potassium iodide in 70 ml of dimethylformamide was stirred at 80° C. for 4.5 hr. The mixture was cooled, filtered and concentrated to an oil, which was stirred with water and extracted with ethyl acetate-ether. The organic extracts were washed with water (2×), saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The mixture was filtered and concentrated. The residue was purified by column chromatography (silica gel, tetrahydrofuran) to give an oil. The oil was converted to 4.5 g (45%) of product by treatment with oxalic acid. Two recrystallizations from ethyl acetate/methanol gave the analytical sample, mp 186°-187° C. (dec).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04609658
출처 데이터셋uspto-grants-1986_09
ORD IDord-ec7fb6350741470a988d0e5ad0be3d81
출처 메모uspto-grants-1986_09