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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81645생성일: 2026년 10월 24일

Dimethylacetamide → 6-{[3-chloro-5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(5-methylpyrazin-2-yl)quinazoline-4-amine

https://huagongshe.com/ko/reaction/81645

반응식

참여 물질

역할이름HCID투입량
반응물DimethylacetamideHCID 31374—
반응물Potassium tert-butoxideHCID 23665647—
반응물3-Chloro-5-(2,2-diethoxyethoxy)-2-fluoropyridineHCID 68427602—
반응물4-((5-Methylpyrazin-2-yl)amino)quinazolin-6-olHCID 135618222—
용매ChloroformHCID 6212—
생성물6-{[3-chloro-5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(5-methylpyrazin-2-yl)quinazoline-4-amineHCID 6842775153%

반응 단계

3-Chloro-5-(2,2-diethoxyethoxy)-2-fluoropyridine (460 mg, 1.74 mmol) and potassium tert-butoxide (160 mg, 1.4 mmol) were added to an N,N-dimethylacetamide suspension (0.9 ml) of 4-[(5-methylpyrazin-2-yl)amino]quinazolin-6-ol (180 mg, 0.71 mmol), and reacted under a nitrogen atmosphere at 200° C. for 30 minutes, using microwaves. The reaction solution was cooled to room temperature, then diluted with chloroform. The organic layer was washed with water 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=96:4) and amine-type silica gel column chromatography (hexane:ethyl acetate=50:50) to obtain 6-{[3-chloro-5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-(5-methylpyrazin-2-yl)quinazoline-4-amine (187 mg, yield: 53%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846700B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-bc572eaa97814650b905e0c3710872ab
출처 메모uspto-grants-2014_09