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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1373281생성일: 2026년 10월 26일

Triphenylphosphine → 4-(2-Chloro-5-methoxyanilino)-5,7-di-(3-morpholinopropoxy)quinazoline

https://huagongshe.com/reaction/1373281

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Di-tert-butyl azodicarboxylateHCID 97268—
반응물3-Morpholino-1-propanolHCID 199576—
반응물4-(2-Chloro-5-methoxyanilino)-7-hydroxy-5-(3-morpholinopropoxy)quinazolineHCID 135830916—
용매DichloromethaneHCID 6344—
생성물4-(2-Chloro-5-methoxyanilino)-5,7-di-(3-morpholinopropoxy)quinazolineHCID 987287231.1%

반응 단계

Di-tert-butyl azodicarboxylate (0.035 g) was added dropwise to a stirred mixture of 4-(2-chloro-5-methoxyanilino)-7-hydroxy-5-(3-morpholinopropoxy)quinazoline (0.045 g), 4-(3-hydroxypropyl)morpholine (0.016 g), triphenylphosphine (0.04 g) and methylene chloride (1 ml). The reaction mixture was stirred at ambient temperature for 10 minutes. The mixture was evaporated and the residue was purified by column chromatography on silica using a 9:10:1 mixture of methylene chloride, ethyl acetate and a saturated methanolic ammonia solution as eluent. The material so obtained was triturated under diethyl ether. The resultant solid was isolated, washed with diethyl ether and dried under vacuum to give the title compound (0.018 g); NMR Spectrum: DMSOd6 and CF3COOD) 2.2–2.4 (m, 4H), 3.15 (m, 4H), 3.35 (m, 4H), 3.5 (m, 4H), 3.7 (m, 4H), 3.8 (s, 3H), 4.02 (t, 4H), 4.35 (t, 2H), 4.6 (t, 2H), 6.95 (s, 1H), 7.03 (s, 1H), 7.05 (m, 1H), 7.5 (s, 1H), 7.6 (d, 1H), 8.88 (s, 1H); Mass Spectrum: M+H+ 572 and 574.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07160891B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-b0004c407c4843788b682da8ae6afe18
출처 메모uspto-grants-2007_01