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HRID 32011作成日:2026年10月24日

Sodium Thiosulfate Pentahydrate → 1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanone

https://huagongshe.com/ja/reaction/32011

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium Thiosulfate PentahydrateHCID 61475—
反応物TriacetoxyperiodinaneHCID 159087—
反応物Sodium BicarbonateHCID 516892—
反応物1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanolHCID 21114171—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物1-[6-(4-Bromo-2-chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanoneHCID 2111417271%

反応手順

A solution of 1-[6-(4-bromo-2-chloro-phenylamino)-7-fluoro-3-methyl-3H-benzoimidazol-5-yl]-2-methoxymethoxy-ethanol 10i (44 mg, 0.096 mmol) and the Dess-Martin periodinane (49 mg, 0.12 mmol) in CH2Cl2 (1.5 mL) is stirred for 1.5 hours at room temperature. The reaction mixture is diluted with ether (3 mL). Saturated aqueous NaHCO3 (1 mL) containing sodium thiosulfate pentahydrate (74 mg) is added. The resulting mixture is stirred for 10 minutes and diluted with EtOAc. The organic layer is washed with saturated aqueous NaHCO3 and brine, dried over MgSO4, filtered, and concentrated in vacuo to give a crude material which is purified by flash chromatography (1.5% MeOH in CH2Cl2) to afford the desired product (31 mg, 71%): MS APCI (+) m/z 456, 458 (M+, Br pattern) detected.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425637B2
出典データセットuspto-grants-2008_09
ORD IDord-e9c32509e51d4cc49e566892f3e4e21e
出典メモuspto-grants-2008_09