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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37096생성일: 2026년 10월 24일

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/ko/reaction/37096

반응식

참여 물질

역할이름HCID투입량
반응물Sodium GlycolateHCID 517347—
반응물SodiumHCID 5360545—
반응물4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamideHCID 19934755—
용매Ethylene GlycolHCID 174—
생성물4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamideHCID 9830283—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420129
출처 데이터셋uspto-grants-1995_05
ORD IDord-8af9041743f64ffb915679f0890fb30c
출처 메모uspto-grants-1995_05