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HRID 1738411作成日:2026年10月25日

Ethyl Acetate → N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]thiophene-2-sulfonamide

https://huagongshe.com/reaction/1738411

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物5-Amino-3,4-dimethylisoxazoleHCID 88317—
反応物1-Benzothiophene-2-sulfonyl chlorideHCID 2776333—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒PyridineHCID 1049—
生成物N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]thiophene-2-sulfonamideHCID 2344548260%

反応手順

3,4-Dimethyl-5-amino-isoxazole (0.224 g, 2.0 mmol) and 50 mg of DMAP were stirred in 5 ml of pyridine at 250 C. The benzo[b]thiophene-2-sulfonyl chloride (0.16 g, 2.6 mmol) was added and the dark brown-yellow reaction mixture was stirred for 18 h at ambient temperature, poured into 100 ml of ethyl acetate and washed with 2% HCl (3×50 ml). The organic phase was dried with MgSO4, filtered and concentrated to collect 0.61 g of a brown oil/solid. The brown oil/solid was subjected to flash chromatography (30% ethyl acetate/hexanes) to provide 0.37 g of a light brown solid. This was stirred in 10 ml of methanol and 0.5 g of NaOH. The methanolic solution was heated for reflux for 1 h, then cooled to 25° C. and the methanol was removed in vacuo. The resulting residue was acidified to pH 1 with 2% HCl (100 ml) and extracted with ethyl acetate (2×50 ml) The organic phase was dried with MgSO4, filtered and concentrated to collect 0.225 g of a yellow-orange solid. This was recrystallized from CHCl3 /hexanes to produce a light tan-yellow solid (0.194 g, 31 % yield), m.p. 157-160° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05962490
出典データセットuspto-grants-1999_10
ORD IDord-39e2c904348a4d519815a5fc54c3b8b9
出典メモuspto-grants-1999_10