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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81628생성일: 2026년 10월 26일

Dimethylacetamide → 6-{[2-(2,2-diethoxyethoxy)pyrimidin-5-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine

https://huagongshe.com/reaction/81628

반응식

참여 물질

역할이름HCID투입량
반응물DimethylacetamideHCID 31374—
반응물4-[(1-Methyl-1H-pyrazol-3-yl)amino]quinazolin-6-olHCID 23160382—
반응물Potassium tert-butoxideHCID 23665647—
반응물2-(2,2-Diethoxyethoxy)-5-fluoropyrimidineHCID 68427683—
용매WaterHCID 962—
생성물6-{[2-(2,2-diethoxyethoxy)pyrimidin-5-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amineHCID 6842885337.6%

반응 조건

온도190 °C

반응 단계

2-(2,2-Diethoxyethoxy)-5-fluoropyrimidine (168 mg, 0.73 mmol) and potassium tert-butoxide (93 mg, 0.83 mmol) were added to an N,N-dimethylacetamide solution (1 ml) of 4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-ol (80 mg, 0.33 mmol), and stirred at 190° C. for 14 hours under a nitrogen atmosphere in a sealed tube. The reaction solution was cooled with ice, water was added, and extracted with chloroform. The organic layer was washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (Moritex, acetone:hexane=1:2) to obtain 6-{[2-(2,2-diethoxyethoxy)pyrimidin-5-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine (56 mg, yield: 37%) as a pale brown amorphous solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846700B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d1e59b377485443ca7fa41e9f0b25ca9
출처 메모uspto-grants-2014_09