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HRID 452681作成日:2026年10月27日

4-Toluenesulfonyl chloride → 6-[5-[2-[3-(Trifluoromethyl)phenyl]ethyl]-1,3,4-oxadiazol-2-yl]benzothiazole

https://huagongshe.com/reaction/452681

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物N'-[3-[3-(trifluoromethyl)phenyl]propionyl]benzothiazole-6-carbohydrazideHCID 68664426—
溶媒PyridineHCID 1049—
溶媒Ethyl AcetateHCID 8857—
生成物6-[5-[2-[3-(Trifluoromethyl)phenyl]ethyl]-1,3,4-oxadiazol-2-yl]benzothiazoleHCID 6866310875%

反応手順

A solution of N′-[3-[3-(trifluoromethyl)phenyl]propionyl]benzothiazole-6-carbohydrazide (433 mg, 1.10 mmol) and p-toluenesulfonyl chloride (419 mg, 2.20 mmol) in pyridine (5 mL) was stirred under an argon atmosphere at 80° C. for 16 hr. After cooling, the reaction mixture was diluted with ethyl acetate, washed with 0.1M hydrochloric acid and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=1/1) and recrystallized from hexane/ethyl acetate to give the title compound (308 mg, yield 75%) as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08492378B2
出典データセットuspto-grants-2013_07
ORD IDord-01ba171fa41440188f5ac899891d28f9
出典メモuspto-grants-2013_07