戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 13290作成日:2026年10月25日

Cesium carbonate → Tert-butyl (3-fluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-phenyl)-carbamate

https://huagongshe.com/reaction/13290

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物tert-Butyl (3-Fluoro-4-hydroxyphenyl)carbamateHCID 11708410—
反応物5-chloro-2-(methylsulfonyl)PyridineHCID 23145229—
溶媒Ethyl AcetateHCID 8857—
生成物Tert-butyl (3-fluoro-4-(6-methanesulfonyl-pyridin-3-yloxy)-phenyl)-carbamateHCID 86619205—

反応条件

温度100 °C

反応手順

4.00 g of 5-chloro-2-methanesulfonyl-pyridine and 8.80 g of cesium carbonate were added to an N-methylpyrrolidinone (50 ml) solution of 4.74 g of tert-butyl (3-fluoro-4-hydroxy-phenyl)-carbamate obtained in (step 1), and the reaction liquid was stirred at 100° C. for 2 hours. The reaction liquid was diluted with ethyl acetate, washed with water and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=1/1) to obtain the entitled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728025B2
出典データセットuspto-grants-2010_06
ORD IDord-f25b9b9defd24663b180c955f8b5d0f7
出典メモuspto-grants-2010_06