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HRID 5460作成日:2026年10月23日

Acetonitrile → 5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridine

https://huagongshe.com/ja/reaction/5460

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Benzenesulfonyl chlorideHCID 7369—
反応物TriethylamineHCID 8471—
反応物5-[3-(Amino)propyloxy]imidazo[1,2-a]pyridine dihydrochlorideHCID 23362997—
溶媒DichloromethaneHCID 6344—
生成物5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridineHCID 2336297859.5%

反応手順

To a suspension of 5-[3-(amino)propyloxy]imidazo[1,2-a]pyridine dihydrochloride (2.64 g, 10 mmoles) and triethylamine (4.88 ml, 35 mmoles) in methylene chloride (100 ml)-acetonitrile (30 ml) was added benzenesulfonyl chloride (1.53 ml, 12 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 1 hour. The reaction mixture was washed in turn with an aqueous sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the crude product thus obtained was recrystallized from methylene-ethanol to obtain 1.97 g of the desired product (59.5%, light brown crystals).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244908
出典データセットuspto-grants-1993_09
ORD IDord-87ae7e60b3f94aeab00f82581b06295a
出典メモuspto-grants-1993_09