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HRID 64873作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/64873

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalic AcidHCID 971—
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物1-(4-Fluorophenyl)piperazineHCID 75260—
反応物3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazoleHCID 10910880—
溶媒DimethylformamideHCID 6228—
生成物1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(4-fluorophenyl)piperazine oxalateHCID 13520733—

反応手順

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, mo 186°-187° C. (dec).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04610988
出典データセットuspto-grants-1986_09
ORD IDord-ab3f0d82e4be403ea50296641c73b690
出典メモuspto-grants-1986_09