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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10249생성일: 2026년 10월 23일

Allyl Alcohol → 4-i-Propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)pyrimidin-4-yl]-amide

https://huagongshe.com/ko/reaction/10249

반응식

참여 물질

역할이름HCID투입량
반응물Allyl AlcoholHCID 7858—
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물4-i-Propyl-phenyl sulfamic acid-[6-chloro-5-(o-methoxy-phenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-amideHCID 10279868—
용매DimethylformamideHCID 6228—
생성물4-i-Propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)pyrimidin-4-yl]-amideHCID 21979588—

반응 조건

온도80 °C

반응 단계

To a mixture of allyl alcohol (1 ml) and THF (2 ml) was added sodium hydride (100 mg, 60% dispersion in mineral oil) followed by the addition of 4-i-propyl-phenyl sulfamic acid-[6-chloro-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (100 mg, Referential Example 1e)). DMF (0.5 ml) was added and the reaction mixture was heated to 80° C. for 20 h. The solvents were evaporated, water (14 ml) and a 10% solution of citric acid was added until the pH was 3. The precipitate was filtered off and washed with water and purified by chromatography through silicagel with EtOAc/Hex=3:2 to give 4-i-propyl-phenyl sulfamic acid-[6-allyloxy-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide (10 mg). tR=5.36 min, (LC); [M+H]+=548.46 (ES+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094781B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-a308b8d7315b46f3a3735372c111dddd
출처 메모uspto-grants-2006_08