戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 37096作成日:2026年10月25日

Sodium Glycolate → 4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide

https://huagongshe.com/reaction/37096

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium GlycolateHCID 517347—
反応物SodiumHCID 5360545—
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Ethylene GlycolHCID 174—
生成物4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamideHCID 9830283—

反応条件

温度80 °C

反応手順

1 g of 4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide was added to a sodium glycolate solution from 2.5 g of ethylene glycol and 0.12 g of sodium. The reaction mixture was stirred at 80° C. under argon for 72 hours. Thereafter, the ethylene glycol was distilled off and the residue was partitioned between ethyl acetate and 1 N hydrochloric acid. The organic phase was washed with water, dried over sodium sulphate and the solvent was distilled off. The residue was chromatographed over silica gel with ether. There was obtained 0.85g of 4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide. m.p 162°-164° C., MS: M=606.

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-8af9041743f64ffb915679f0890fb30c
出典メモuspto-grants-1995_05