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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1517295생성일: 2026년 10월 26일

Ammonium Chloride → 6-{[3-chloro-5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-pyrazin-2-ylquinazoline-4-amine

https://huagongshe.com/reaction/1517295

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Potassium tert-butoxideHCID 23665647—
반응물2,3-Dichloro-5-(2,2-diethoxyethoxy)pyridineHCID 86645896—
반응물4-(Pyrazin-2-ylamino)quinazolin-6-olHCID 136334744—
용매DimethylacetamideHCID 31374—
생성물6-{[3-chloro-5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-pyrazin-2-ylquinazoline-4-amineHCID 6843065710%

반응 조건

온도200 °C

반응 단계

2,3-Dichloro-5-(2,2-diethoxyethoxy)pyridine (810 mg, 2.9 mmol) and potassium tert-butoxide (350 mg, 3.1 mmol) were added to an N,N-dimethylacetamide suspension (3 ml) of 4-(pyrazin-2-ylamino)quinazolin-6-ol (300 mg, 1.25 mmol), and stirred for 24 hours in a sealed tube at 200° C. The reaction solution was cooled to room temperature, aqueous saturated ammonium chloride solution was added, filtered, and washed with a mixed solution of chloroform/methanol (9:1). The obtained filtrate was extracted 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 reversed-phase liquid chromatography (YMC CombiPrep Pro C18 AS-360-cc) to obtain 6-{[3-chloro-5-(2,2-diethoxyethoxy)pyridin-2-yl]oxy}-N-pyrazin-2-ylquinazoline-4-amine (60 mg, yield: 10%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08232284B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-68f6597666cc47cc8fb60bd3aa486712
출처 메모uspto-grants-2012_07