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HRID 459008作成日:2026年10月26日

Triethylamine → Methanesulfonic acid (5R)-3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

https://huagongshe.com/reaction/459008

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Compound 3HCID 20788885—
溶媒DichloromethaneHCID 6344—
溶媒Sodium BicarbonateHCID 516892—
生成物Methanesulfonic acid (5R)-3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl esterHCID 2362470598.4%

反応手順

(5R)-3-(3-Fluoro-4-iodophenyl)-5-(hydroxymethyl)-1,3-oxazolidin-2-one (Intermediate 3, 25.0 g, 74.2 mmol) was stirred in dichloromethane (250 ml) at 0° C. Triethylamine (10.5 g, 104 mmol) was added followed by methanesulfonyl chloride (11.2 g, 89.0 mmol) and the reaction was stirred overnight, slowly warming to room temperature. The yellow solution was diluted with sodium bicarbonate and the compound was extracted using dichloromethane (3×250 ml). The organic layer was dried (magnesium sulfate), filtered and concentrated to give the desired product as a light yellow solid (30.3 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07192974B2
出典データセットuspto-grants-2007_03
ORD IDord-0a37313cf2d845e8aa645def85d8fbaf
出典メモuspto-grants-2007_03