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HRID 1814111作成日:2026年10月27日

(1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)(thiazol-2-yl)-methanol → 1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(2-thiazolylcarbonyl)indole

https://huagongshe.com/reaction/1814111

反応式

関与物質

役割名称HCID仕込み量
反応物(1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)(thiazol-2-yl)-methanolHCID 22504451—
触媒HCID 178418406HCID 178418406—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Fluorobenzyl)-5-methanesulfonyl-2-(2-thiazolylcarbonyl)indoleHCID 2250442245.7%

反応手順

To a solution of the compound obtained in Example 27 (5) (110 mg) in dichloromethane (20 ml), manganese dioxide (900 mg) was added at 15 to 30° C. and the mixture was stirred for 30 minutes. The reaction solution was then filtered through Celite and concentrated under reduced pressure. The resulting residue was subjected to silica gel preparative thin-layer chromatography (hexane:ethyl acetate=1:1) to obtain 50 mg of the desired products as a yellow powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06875770B2
出典データセットuspto-grants-2005_04
ORD IDord-209eb3bf37fd4423927b1bc3fc381db0
出典メモuspto-grants-2005_04