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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 326708생성일: 2026년 10월 24일

Sodium Glycolate → N-[6-(2-hydroxy-ethoxy)-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfon-amide

https://huagongshe.com/ko/reaction/326708

반응식

참여 물질

역할이름HCID투입량
반응물Sodium GlycolateHCID 517347—
반응물SodiumHCID 5360545—
반응물N-[6-chloro-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfonamideHCID 19735459—
용매Ethylene GlycolHCID 174—
생성물N-[6-(2-hydroxy-ethoxy)-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfon-amideHCID 19735450—

반응 단계

190 mg of N-[6-chloro-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfonamide were added to a sodium glycolate solution from 46 mg of sodium in 1 ml of ethylene glycol. After a reaction period of 5 hours at 100° C., the reaction mixture was evaporated to dryness under reduced pressure. The residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic phase was washed neutral, dried and evaporated under reduced pressure. The residue was chromatographed on silica gel with methylene chloride and ethyl acetate (4:1 v/v). There were obtained 175 mg of N-[6-(2-hydroxy-ethoxy)-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfon-amide, melting point 147°-149° C. (from methylene chloride/hexane).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05270313
출처 데이터셋uspto-grants-1993_12
ORD IDord-e2b486f0faba44978e09600883630e9b
출처 메모uspto-grants-1993_12