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HRID 328338作成日:2026年10月26日

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

https://huagongshe.com/reaction/328338

反応式

関与物質

役割名称HCID仕込み量
反応物ThiabendazoleHCID 5430—
反応物Benzylthiocarbonyl chlorideHCID 19906501—
溶媒PyridineHCID 1049—
生成物1-Benzylthiocarbonyl-2-(4-thiazolyl)-benzimidazoleHCID 54052980—

反応手順

17.0 G. (0.091 moles) of benzylthiocarbonyl chloride is added dropwise under anhydrous conditions over a period of 25 minutes to a stirred suspension of 18.3 g. (0.091 moles) of 2-(4-thiazolyl)-benzimidazole in 140 ml. of pyridine. All of the solid material dissolved before the completion of the addition. When the addition is complete, precipitation of pyridine hydrochloride commences. The reaction mixture is stirred at room temperature for 18 hours, filtered and the pyridine solution evaporated to dryness in vacuo. The residue is dissolved in 250 ml. of methylene chloride filtered and the filtrate washed twice with 250 ml. of 0.25 normal hydrochloric acid and 200 ml. of saturated sodium bicarbonate solution. The methylene chloride is dried, treated with charcoal, filtered and evaporated to dryness in vacuo affording a solid material which is recrystallized from toluene affording 14.3 g. (45%) of 1-benzylthiocarbonyl-2-(4-thiazolyl)-benzimidazole, melting point 122° to 123° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04017505
出典データセットuspto-grants-1977_04
ORD IDord-b31944e15c4d4e3e84661abbfc3d4d7e
出典メモuspto-grants-1977_04