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2-Hydroxy-5-methoxybenzophenone → HCID 24879062, 화합물

HRID 228594
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인쇄 미리보기

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HRID 228594 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:14][CH3:15])=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][CH:3]=1.[OH:16][C:17]1[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][C:18]=1[C:19]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:20]>>[CH3:13][O:12][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][C:8]=1[O:14][CH3:15])[N:5]=[CH:4][CH:3]=[C:2]2[O:16][C:17]1[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][C:18]=1[C:19]([C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)=[O:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 268812-Hydroxy-5-methoxybenzophenoneHCID 4596104-Chloro-6,7-dimethoxyquinoline

생성물 1

HCID 24879062HCID 24879062, 화합물수율 8.1%

반응 조건

온도
180 °C

실험 절차

A mixture of 4-chloro-6,7-dimethoxyquinoline (93 mg) with 2-hydroxy-5-methoxybenzophenone (462 mg) was stirred at 180° C. for 9 hr. The reaction solution was cooled to room temperature and was purified by column chromatography on silica gel using acetone-hexane to give the title compound (14 mg, yield 8%).

후처리

  1. temperatureThe reaction solution was cooled to room temperature
  2. customwas purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-2e4e47a6537841959febb3d150c4557e
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07560558B2

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