돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1517283생성일: 2026년 10월 25일

Potassium tert-butoxide → 6-{[5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(5-methylpyrazin-2-yl)quinazoline-4-amine

https://huagongshe.com/reaction/1517283

반응식

참여 물질

역할이름HCID투입량
반응물Potassium tert-butoxideHCID 23665647—
반응물5-(2,2-Diethoxyethoxy)-2-fluoropyridineHCID 68429706—
반응물4-((5-Methylpyrazin-2-yl)amino)quinazolin-6-olHCID 135618222—
용매Dimethyl SulfoxideHCID 679—
생성물6-{[5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(5-methylpyrazin-2-yl)quinazoline-4-amineHCID 6842907080.1%

반응 조건

온도130 °C

반응 단계

5-(2,2-Diethoxyethoxy)-2-fluoropyridine (680 mg, 3.0 mmol) and potassium tert-butoxide (670 mg, 5.9 mmol) were added to a dimethyl sulfoxide solution (10 ml) of 4-[(5-methylpyrazin-2-yl)amino]quinazolin-6-ol (500 mg, 1.97 mmol), and stirred under a nitrogen atmosphere at 130° C. for 24 hours. The reaction solution was cooled to room temperature, and extracted with a mixed solution of chloroform/methanol (9:1). The organic layer was washed with aqueous saturated ammonium chloride solution and saturated saline water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform:methanol=95:5) to obtain 6-{[5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(5-methylpyrazin-2-yl)quinazoline-4-amine (730 mg, yield: 80%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08232284B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-7a0944affe964f629f2be8f8efc40b9e
출처 메모uspto-grants-2012_07