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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-(3-Benzyloxy-5-methoxyphenyl)-6,7-methylenedioxyquinolin-4-one → 2-(3-Hydroxy-5-methoxyphenyl)-6,7-methylenedioxyquinolin-4-one

HRID 38660
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인쇄 미리보기

반응식

HRID 38660 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([C:17]2[CH2:26][C:25](=[O:27])[C:24]3[C:19](=[CH:20][C:21]4[O:30][CH2:29][O:28][C:22]=4[CH:23]=3)[N:18]=2)[CH:12]=[C:13]([O:15]C)[CH:14]=1)C1C=CC=CC=1>CO.[Pd]>[OH:15][C:13]1[CH:12]=[C:11]([C:17]2[CH2:26][C:25](=[O:27])[C:24]3[C:19](=[CH:20][C:21]4[O:30][CH2:29][O:28][C:22]=4[CH:23]=3)[N:18]=2)[CH:10]=[C:9]([O:8][CH3:1])[CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 666594662-(3-Benzyloxy-5-methoxyphenyl)-6,7-methylenedioxyquinolin-4-one

생성물 1

HCID 666595082-(3-Hydroxy-5-methoxyphenyl)-6,7-methylenedioxyquinolin-4-one수율 77%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A suspension of 0.5 g (1.245 mmol) of 165 and 0.25 g of palladium (10 wt % on activated carbon) in 60 mL of methanol was stirred at room temperature under hydrogen gas atmosphere for 24 h. The precipitate were collected and dissolved in 10% NaOH solution and then filtered. The filtrate was acidified with dil aq HCl and the precipitate was then collected and washed with acetone and water to give 166.

후처리

  1. customThe precipitate were collected
  2. dissolutiondissolved in 10% NaOH solution
  3. filtrationfiltered
  4. customthe precipitate was then collected
  5. washwashed with acetone and water

출처 및 근거

ORD 기록
ord-b3283e0473644294a2c1891d17746257
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524740B2

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