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HRID 37102作成日:2026年10月25日

Phenol → 4-tert.-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-2-morpholin-4-yl-6-phenoxymethyl-pyrimidin-4-yl]benzenesulphonamide

https://huagongshe.com/reaction/37102

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物Sodium HydroxideHCID 14798—
反応物Phenolate SodiumHCID 4445035—
反応物4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamideHCID 19934755—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物4-tert.-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-2-morpholin-4-yl-6-phenoxymethyl-pyrimidin-4-yl]benzenesulphonamideHCID 19934777—

反応条件

温度80 °C

反応手順

0.145 g of 4-tert.-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]benzenesulphonamide (Example 4) in 3 ml of acetone was added to a sodium phenolate solution from 0,024 g of phenol and 0.06 g of NaOH in 2 ml of acetone and 1 ml of water. The reaction mixture was stirred at 80° C. under argon for 48 hours. Thereafter, the acetone was distilled off and the residue was partitioned between chloroform and water. The chloroform phase was washed with water, dried over sodium sulphate and the solvent was distilled off. The residue was chromatographed over silica gel with chloroform. 0.07 g of 4-tert.-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-2-morpholin-4-yl-6-phenoxymethyl-pyrimidin-4-yl]benzenesulphonamide, MS: M=639, was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420129
出典データセットuspto-grants-1995_05
ORD IDord-d0aa28ba710c4f8cadc523ef1d3f73ae
出典メモuspto-grants-1995_05