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HRID 20627作成日:2026年10月26日

Pyridine → 8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-yl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/20627

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物8-(cyclopentyloxy)-4-hydroxy-7-methoxy-2H-chromen-2-oneHCID 77174792—
溶媒DichloromethaneHCID 6344—
生成物8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-yl 4-methylbenzenesulfonateHCID 86618132—

反応手順

4-Methylbenzene-1-sulfonyl chloride (135 mg, 0.71 mmol) was added to a solution of 8-(cyclopentyloxy)-4-hydroxy-7-methoxy-2H-chromen-2-one (175 mg, 0.63 mmol), pyridine (0.15 mL, 1.85 mmol), and anhydrous dichloromethane (4 mL) at rt under N2. After 20 h, the reaction was concentrated and purified by silica gel chromatography (1:0→7:3; hexanes:ethyl acetate) to give 8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-yl 4-methylbenzenesulfonate: MS (ESI): 431.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745646B2
出典データセットuspto-grants-2010_06
ORD IDord-5723064d63964d548591af3a350eda5e
出典メモuspto-grants-2010_06