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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(+/-)-2a,5-Dihydropyrrolo[4,3,2-de]quinoline-2,4(1H,3H)-dione → Pyrrolo[4,3,2-de]quinoline-2,4(1H,5H)-dione

HRID 551006
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인쇄 미리보기

반응식

HRID 551006 반응식
[NH:1]1[C:11]2[C:12]3[CH:3]([CH2:4][C:5](=[O:13])[NH:6][C:7]=3[CH:8]=[CH:9][CH:10]=2)[C:2]1=[O:14]>C1(C)C=CC=CC=1.[O-2].[Mn+4].[O-2]>[NH:1]1[C:11]2[C:12]3[C:3](=[CH:4][C:5](=[O:13])[NH:6][C:7]=3[CH:8]=[CH:9][CH:10]=2)[C:2]1=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 57663743(+/-)-2a,5-Dihydropyrrolo[4,3,2-de]quinoline-2,4(1H,3H)-dione

생성물 1

HCID 57663757Pyrrolo[4,3,2-de]quinoline-2,4(1H,5H)-dione

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 1140Toluene용매

실험 절차

A mixture of (±)-2a,5-dihydropyrrolo[4,3,2-de]quinoline-2,4(1H,3H)-dione from Step C (200 mg, 1.06 mmol), and manganese (IV) oxide (185 mg, 2.13 mmol) was heated in toluene (3 mL) at 110° C. for 1 h. The mixture was filtered through a pad of Celite, washing with CH2Cl2:MeOH, and the filtrate was concentrated in vacuo to give the title compound. MS: m/z=187 (M+1).

후처리

  1. filtrationThe mixture was filtered through a pad of Celite
  2. washwashing with CH2Cl2
  3. concentrationMeOH, and the filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-cc786cdc1b114db4b9f4df0fd5523b83
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07947677B2

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