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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454083생성일: 2026년 10월 25일

Triphenylphosphine → 4-(2-Methylindol-5-yloxy)-7-(3-(pyrrolidin-yl)propoxy)quinazoline

https://huagongshe.com/reaction/454083

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물1-PyrrolidinepropanolHCID 209342—
반응물7-Hydroxy-4-(2-methylindol-5-yloxy)quinazolineHCID 135763114—
용매DichloromethaneHCID 6344—
생성물4-(2-Methylindol-5-yloxy)-7-(3-(pyrrolidin-yl)propoxy)quinazolineHCID 2203082335.8%

반응 단계

Diisopropyl azodicarboxylate (146 mg, 0.72 mmol) was added to a solution of 7-hydroxy-4-(2-methylindol-5-yloxy)quinazoline (100 mg, 0.34 mmol), triphenyl phosphine (189 mg, 0.72 mol), and 3-pyrrolidinopropan-1-ol (89 mg, 0.686 mmol), (J. Org. Chem. 1988, 53, 3164), in methylene chloride (2.5 ml). After stirring overnight at ambient temperature, the solid was filtered. The filtrate was purified by column chromatography eluting with ethyl acetate/methylene chloride (1/1) followed by ethyl acetate/methylene chloride/methanol (4/5/1), methylene chloride/methanol (9/1) and 3N ammonia in methanol/methylene chloride (1/9). After removal of the solvent, the residue was triturated with ether, filtered, and dried under vacuum to give 4-(2-methylindol-5-yloxy)-7-(3-(pyrrolidin-yl)propoxy)quinazoline (49 mg, 35%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492560B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-e98edf82ec354b419fca0bd04427b408
출처 메모uspto-grants-2013_07