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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10250생성일: 2026년 10월 25일

Ethylene Glycol → 4-i-Propyl-phenyl sulfamic acid-[6-(2-hydroxy-ethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide

https://huagongshe.com/reaction/10250

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물Sodium hydrideHCID 24758—
반응물4-i-Propyl-phenyl sulfamic acid-[6-chloro-5-(o-methoxy-phenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-amideHCID 10279868—
용매1,2-DimethoxyethaneHCID 8071—
생성물4-i-Propyl-phenyl sulfamic acid-[6-(2-hydroxy-ethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amideHCID 10302811—

반응 조건

온도80 °C

반응 단계

Sodium hydride (17 mg, 60% dispersion in mineral oil) was added to ethylene glycol (1.2 ml) followed by addition of dimethoxyethane (0.5 ml). Stirring was continued for 30 min, then 4-i-propyl-phenyl sulfamic acid-[6-chloro-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (45 mg, Referential Example 1e)) was added and the reaction mixture was heated to 80° C. for 48 h. The solvents were evaporated, water (10 ml) and a 10% solution of citric acid was added until the pH was 3 followed by extraction with EtOAc. The organic layers were dried over sodium sulfate and the solvent was evaporated. The crude product was purified by chromatography through silicagel with EtOAc to give 4-i-propyl-phenyl sulfamic acid-[6-(2-hydroxy-ethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (38 mg). tR=4.56 min, (LC); [M+H]+=552.36 (ES+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094781B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-dd381fa9f51b40b4a02d97a29218a03d
출처 메모uspto-grants-2006_08