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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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6-Hydroxyquinoline → HCID 47453787, 화합물

HRID 2264605
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HRID 2264605 반응식
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][CH:6]=[CH:5]2.[NH2:12][C:13]1[N:18]=[C:17](Cl)[CH:16]=[C:15]([Cl:20])[N:14]=1.[OH-].[Na+]>O.CC(C)=O>[Cl:20][C:15]1[CH:16]=[C:17]([O:1][C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[N:8]=[CH:7][CH:6]=[CH:5]3)[N:18]=[C:13]([NH2:12])[N:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 113746-HydroxyquinolineHCID 14798Sodium HydroxideHCID 655222-Amino-4,6-dichloropyrimidine

생성물 1

HCID 47453787HCID 47453787, 화합물

시약·촉매·용매 1

HCID 18366337Propan-2-one--water (1/1)용매

실험 절차

To a mixture containing 7.25 g (0.05 mol) 6-hydroxy-quinoline, 8.25 g (0.05 mol) 2-amino-4,6-dichloropyrimidine in 300 mL of water/acetone 1:1 are added 2.0 g (0.05 mol) sodium hydroxide. On heating a clear solution is first obtained from which a thick precipitate separates. Stirring under reflux is continued for a total of 6 h. The mixture is cooled, filtered and the solid washed with acetone/water 1.1 and dried. The title compound is obtained as a solid: map. 248-250° C.; MS: [M+1]+=273; HPLC: CtRet=1.30; TLC (dichloromethane/methanol 95:5): Rf=0.46.

후처리

  1. temperatureOn heating a clear solution
  2. customis first obtained from which a thick precipitate separates
  3. temperatureunder reflux
  4. customis continued for a total of 6 h
  5. temperatureThe mixture is cooled
  6. filtrationfiltered
  7. washthe solid washed with acetone/water 1.1
  8. customdried

출처 및 근거

ORD 기록
ord-ab92d23a13344278bed362708f006b64
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07855215B2

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