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3-Fluoroaniline → 6-((3-Fluorophenyl)amino)-5,8-quinoxalinedione

HRID 1153733
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반응식

HRID 1153733 반응식
[OH:1][C:2]1[CH:11]=[CH:10][C:9]([OH:12])=[C:8]2[C:3]=1[N:4]=[CH:5][CH:6]=[N:7]2.[F:13][C:14]1[CH:15]=[C:16]([CH:18]=[CH:19][CH:20]=1)[NH2:17]>[Ag-]=O.C(O)C>[F:13][C:14]1[CH:15]=[C:16]([CH:18]=[CH:19][CH:20]=1)[NH:17][C:10]1[C:9](=[O:12])[C:8]2[N:7]=[CH:6][CH:5]=[N:4][C:3]=2[C:2](=[O:1])[CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 97423-FluoroanilineHCID 1356973965,8-Quinoxalinediol

생성물 1

HCID 1244696-((3-Fluorophenyl)amino)-5,8-quinoxalinedione

시약·촉매·용매 2

HCID 178418778HCID 178418778, 화합물촉매HCID 702Ethanol용매

실험 절차

Approximately one gram of 5,8-dihydroxyquinoxaline was dissolved in 100 ml. of 2B ethanol. To the solution were added about 5 g. of freshly prepared silver (I) oxide and about 3 g. of 3-fluoroaniline. The reaction was stirred overnight at room temperature and worked up in the same manner as described in Example 3. Crystallization from ethyl acetate gave about 500 mg. of the title compound.

후처리

  1. additionTo the solution were added about 5 g
  2. customCrystallization from ethyl acetate
  3. customgave about 500 mg

출처 및 근거

ORD 기록
ord-7171877cfe2b47b1bae01f044166c85b
출처 데이터셋
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04486432

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