戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 902872作成日:2026年10月25日

Water → 5-(benzenesulfonyl)-4,6-dihydro-5H-pyrrolo[3,4-d]thiazole

https://huagongshe.com/reaction/902872

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物BenzenesulfonamideHCID 7370—
反応物Sodium hydrideHCID 24758—
反応物4,5-Bis(bromomethyl)thiazoleHCID 10849698—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物5-(benzenesulfonyl)-4,6-dihydro-5H-pyrrolo[3,4-d]thiazoleHCID 18442806—

反応手順

Benzenesulfonamide (638 mg) and 4,5-bis(bromomethyl)thiazole (M. Al. Hariri, O. Galley, F. Pautet, H. Fillion, Eur. J. Org. Chem., 1998, 593-594.) (1.10 g) were dissolved in N,N-dimethylformamide (10 ml), sodium hydride (60% in oil, 357 mg) was added at a time, and the mixture was stirred at room temperature for 3 hours. Water and methylene chloride were added to conduct liquid separation. After the resultant organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off, and the residue was purified by column chromatography on silica gel (methylene chloride:ethyl acetate=9:1) to obtain the title compound (137 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07365205B2
出典データセットuspto-grants-2008_04
ORD IDord-39e55d46c1b1468caadb96261d27420d
出典メモuspto-grants-2008_04