돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 639961생성일: 2026년 10월 26일

Triphenylphosphine → 4-Chloro-7-(3-chloropropoxy)-6-methoxyquinazoline

https://huagongshe.com/reaction/639961

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-Chloro-1-propanolHCID 12313—
반응물Di-tert-butyl azodicarboxylateHCID 97268—
반응물4-Chloro-6-methoxyquinazolin-7-olHCID 135742251—
용매DichloromethaneHCID 6344—
생성물4-Chloro-7-(3-chloropropoxy)-6-methoxyquinazolineHCID 5744722791%

반응 단계

Triphenylphosphine (2.6 g, 10.1 mmol) and 3-chloropropanol (0.69 ml, 8.2 mmol) were added to a suspension of 4-chloro-7-hydroxy-6-methoxyquinazoline (1.65 g, 7.8 mmol) in dichloromethane (100 ml) under argon. The flask was placed in a water bath at 20° C. and di-tertbutyl azodicarboxylate (2.30 g, 10.1 mmol) added portion wise over a few minutes. The reaction mixture was stirred at ambient temperature for 2 hours. The reaction mixture was concentrated and the solution loaded directly onto a silica chromatography column. Elution with ethyl acetate:petroleum ether (3:7), yielded 4-chloro-7-(3-chloropropoxy)-6-methoxyquinazoline (2.0 g, 91% yield):

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691867B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-eb7626e449e04f46aadfe370377ff9e0
출처 메모uspto-grants-2010_04