戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 326712作成日:2026年10月26日

Ethylene Glycol → N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide

https://huagongshe.com/reaction/326712

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物Sodium GlycolateHCID 517347—
反応物SodiumHCID 5360545—
反応物HCID 12396954HCID 12396954—
生成物N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamideHCID 19735392—

反応条件

温度125 °C

反応手順

300 mg of N-[6-chloro-5-(p-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide were added to a sodium glycolate solution from 1 ml of dry ethylene glycol and 46 mg of sodium. The reaction mixture was heated at 125° C. for 4 hours under an argon atmosphere. Thereafter, the ethylene glycol was distilled under reduced pressure. The residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic phase was washed neutral, dried and evaporated. The residue was chromatographed on silica gel with methylene chloride/ethyl acetate (1:1 v/v). There were obtained 250 mg of N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide, melting point 161°-162° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05270313
出典データセットuspto-grants-1993_12
ORD IDord-e0b87538e9714a53aab5aecb6702ad63
出典メモuspto-grants-1993_12