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HRID 232753作成日:2026年10月27日

5-Amino-3,4-dimethylisoxazole → N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]furan-2-sulfonamide

https://huagongshe.com/reaction/232753

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-3,4-dimethylisoxazoleHCID 88317—
反応物1-Benzofuran-2-sulfonyl chlorideHCID 2795172—
生成物N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]furan-2-sulfonamideHCID 22998530—

反応手順

N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]furan-2-sulfonamide was prepared, in the same manner as described in Example 34B, from 3,4-dimethyl-5-amino isoxazole (78 mg, 0.70 mmol) and benzo[b]furan-2-sulfonyl chloride (0.46 g, 2.1 mmol) Flash chromatography (30% ethyl acetate/hexanes) provided 0.186 g of a light yellow solid, which was treated with 31 mg of NaOH in 10 ml of methanol at 25° C. for 30 minutes. Recrystallization from CHCl3 /hexanes yielded a light tan solid (90 mg, 44% yield), m.p. 160.5°-163° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05591761
出典データセットuspto-grants-1997_01
ORD IDord-665bfcd8fbcf47f79334d37afc6b5139
出典メモuspto-grants-1997_01