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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81625생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/81625

반응식

참여 물질

역할이름HCID투입량
반응물DimethylacetamideHCID 31374—
반응물4-[(1-Methyl-1H-pyrazol-3-yl)amino]quinazolin-6-olHCID 23160382—
반응물Potassium tert-butoxideHCID 23665647—
반응물5-(2,2-Diethoxyethoxy)-2-fluoropyridineHCID 68429706—
용매WaterHCID 962—
생성물6-{[5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amineHCID 6842977565%

반응 조건

온도170 °C

반응 단계

5-(2,2-diethoxyethoxy)-2-fluoropyridine (502 mg, 2.19 mmol) and potassium tert-butoxide (279 mg, 2.49 mmol) were added to an N,N-dimethylacetamide solution (1 ml) of 4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-ol (240 mg, 1.00 mmol), and stirred at 170° C. for 15 hours under a nitrogen atmosphere in a sealed tube. The reaction solution was cooled to room temperature, then 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 (Biotage, chloroform:methanol=100:3) to obtain 6-{[5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine (292 mg, yield: 65%) as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846700B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c6d2e65ddbf94c72b551a36e2c02a94f
출처 메모uspto-grants-2014_09