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HRID 1900714作成日:2026年10月27日

Ethanol → 2-Methanesulfonyloxymethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one

https://huagongshe.com/reaction/1900714

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物PyridineHCID 1049—
反応物Methanesulfonyl chlorideHCID 31297—
反応物2-Hydroxymethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-oneHCID 23369679—
溶媒MethanolHCID 887—
溶媒ChloroformHCID 6212—
生成物2-Methanesulfonyloxymethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-oneHCID 23369644—

反応手順

2-Hydroxymethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one (1.2 g) was added to anhydrous pyridine (24 ml). The mixture was stirred on ice, during which methanesulfonylchloride (625 mg) was added thereto, followed by stirring at room temperature for 100 minutes. Methanesulfonylchloride (283 mg) was added again and stirred at the same temperature for 50 minutes. After completion of the reaction, a small amount of ethanol was added, and the mixture was brought to dryness under reduced pressure. The residue was dissolved in a solvent mixture of chloroform and methanol (10:1), washed with diluted HCl, sodium bicarbonate water, and aqueous NaCl solution in this order, and dried. When the solvent was evaporated, 1.6 g (quantitative assay) of the title compound was obtained. This substance was recrystallized from a solvent mixture of chloroform-n-hexane, obtaining colorless powdery crystals having a melting point of 200°-203° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05576324
出典データセットuspto-grants-1996_11
ORD IDord-9e9d94a0bfea42afa73dedfc4b5b02f5
出典メモuspto-grants-1996_11