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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52618생성일: 2026년 10월 24일

Quinazoline → 2,4-Diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline

https://huagongshe.com/ko/reaction/52618

반응식

참여 물질

역할이름HCID투입량
반응물QuinazolineHCID 9210—
반응물Boron tribromideHCID 25134—
반응물2,4-Diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazolineHCID 54072668—
용매DichloromethaneHCID 6344—
생성물2,4-Diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazolineHCID 54369095—

반응 단계

A series of quinazoline analogs may be prepared from the above 2,4-diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazoline. This is accomplished by the reaction of 2,4-diamino-5-chloro-6-(5-chloro-2-methoxyphenyl)quinazoline with 1M boron tribromide in methylene chloride, yielding the corresponding 2,4-diamino-5-chloro-6-(5-chloro-2-hydroxyphenyl)quinazoline. The hydroxy intermediate in turn is reacted with a halogen-containing compound and potassium carbonate in N,N-dimethylformamide, affording the appropriately 6-(5-chloro-2-substituted-phenyl)quinazoline, for example, 2,4-diamino-5-chloro-6-[5-chloro-2-(pyridin-2-ylmethoxy)phenyl]quinazoline. Example 3 describes in detail the preparation of this compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616718
출처 데이터셋uspto-grants-1997_04
ORD IDord-7bbc177f69574626b20c30222e1109fd
출처 메모uspto-grants-1997_04