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HRID 328333作成日:2026年10月27日

Thiabendazole → 1-(2-Benzyloxyethoxycarbonyl)-2-(4-thiazolyl)-benzimidazole

https://huagongshe.com/reaction/328333

反応式

関与物質

役割名称HCID仕込み量
反応物ThiabendazoleHCID 5430—
反応物2-Benzyloxyethyl chloroformateHCID 4563900—
反応物Pyridinium chlorideHCID 10176127—
溶媒PyridineHCID 1049—
生成物1-(2-Benzyloxyethoxycarbonyl)-2-(4-thiazolyl)-benzimidazoleHCID 21441722—

反応手順

32.2 G. (150 mmoles) of 2-benzyloxyethylchloroformate is added dropwise with protection from moisture to a stirred suspension of 30.1 g. (150 mmoles) of 2(4-thiazolyl)-benzimidazole in 200 ml. of pyridine. The addition is complete in 30 minutes whereupon all of the starting material is dissolved and pyridine hydrochloride begins to precipitate. The reaction mixture is stirred at room temperature for 15 1/2 hours and filtered to remove pyridine hydrochloride. The solid material is washed with a small volume of pyridine and the combined filtrate and washing are evaporated to dryness in vacuo. The residual oil is dissolved in 300 ml. of methylene chloride and allowed to stand during which time a substantial amount of solid material precipitates. The solid is removed by filtration and the filtrate washed twice with 250 ml. of 0.25 N HCl containing ice followed by 200 ml. of saturated sodium bicarbonate solution containing 50 ml. of ice. The methylene chloride fraction is dried with magnesium sulfate, treated with charcoal, filtered and evaporated to dryness in vacuo affording 38.9 g. of a yellow-orange oil which begins to solidify on standing. The material is recrystallized from toluenecyclohexane affording 23.8 g. of 1-(2-benzyloxyethoxycarbonyl)-2-(4-thiazolyl)-benzimidazole, m.p. 93°-95° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04017503
出典データセットuspto-grants-1977_04
ORD IDord-179c30dd96af4d33bcc359b2436b5e89
出典メモuspto-grants-1977_04