돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228918생성일: 2026년 10월 25일

Water → Propyl 3-(7-benzyloxy-6-methoxy-quinolin-4-yloxy)naphthalene-2-carboxylate

https://huagongshe.com/reaction/228918

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Propyl 2-hydroxy-3-naphthoateHCID 250121—
반응물7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 22646562—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매1,2-DichlorobenzeneHCID 7239—
생성물Propyl 3-(7-benzyloxy-6-methoxy-quinolin-4-yloxy)naphthalene-2-carboxylateHCID 2307840150.1%

반응 조건

온도120 °C

반응 단계

Propyl 3-hydroxy-naphthalene-2-carboxylate (460 mg), 7-benzyloxy-4-chloro-6-methoxyquinoline (200 mg), and 4-dimethylaminopyridine (244 mg) were suspended in o-dichlorobenzene (4 ml), and the mixture was stirred at 120° C. for 5 hr. The reaction solution was cooled to room temperature, water was then added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was washed with saturated brine and was dried over anhydrous sodium sulfate, the solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using chloroform-acetone to give propyl 3-(7-benzyloxy-6-methoxy-quinolin-4-yloxy)-naphthalene-2-carboxylate (165 mg, yield 50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-168e7c6ed7eb4d059e106f9b82f305a0
출처 메모uspto-grants-2009_07