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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Quinoline → HCID 178516370, 화합물

HRID 1013624
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HRID 1013624 반응식
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([OH:15])=[C:7](C(O)=O)[CH:8]=[N:9]2)=[N:4][CH:3]=1.N1C2C(=CC=CC=2)C=CC=1>CC(C)=O>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([OH:15])=[CH:7][CH:8]=[N:9]2)=[N:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7047QuinolineHCID 178524700HCID 178524700, 화합물

생성물 1

HCID 178516370HCID 178516370, 화합물수율 88.9%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

In a RBF fitted with a reflux condenser, 7-bromo-4-hydroxy-1,5-naphthyridine-3-carboxylic acid (1 g, 4 mmol) was added in portions over 10 minutes to stirred refluxing quinoline (50 mL), and the resulting mixture was refluxed for 1 h. The mixture was cooled and diluted with acetone. The precipitate was filtered, washed with water and dried to give 0.8 g of a grey-brown powder. The product was reprecipitated from aq. NaOH with glacial acetic acid to give a white solid.

후처리

  1. customIn a RBF fitted with a reflux condenser
  2. temperaturethe resulting mixture was refluxed for 1 h
  3. temperatureThe mixture was cooled
  4. filtrationThe precipitate was filtered
  5. washwashed with water
  6. customdried

출처 및 근거

ORD 기록
ord-310bbe64cd734a8f9dffaf9bfd3d6ae2
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981891B2

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