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Oxalyl chloride → 7-fluoro-1-(2-fluoro-phenyl)-3-methyl-1H-quinolin-4-one

HRID 1887811
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HRID 1887811 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:11])[CH2:9][CH3:10])=[C:4]([NH:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[F:19])[CH:3]=1.[C:20](Cl)(=O)C(Cl)=O>CN(C=O)C>[F:1][C:2]1[CH:3]=[C:4]2[C:5]([C:8](=[O:11])[C:9]([CH3:20])=[CH:10][N:12]2[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[F:19])=[CH:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 65578Oxalyl chlorideHCID 712084951-[4-Fluoro-2-(2-fluoro-phenylamino)-phenyl]-propan-1-one

생성물 1

HCID 712089357-fluoro-1-(2-fluoro-phenyl)-3-methyl-1H-quinolin-4-one수율 37.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
0 °C

실험 절차

In a 250 mL round bottom flask, 1-[4-fluoro-2-(2-fluoro-phenylamino)-phenyl]-propan-1-one (3.05 g, 11.7 mmol) was added to DMF (4.3 mL) at 0° C. Oxalyl chloride (8.18 mL, 96.7 mmol) was added slowly and the reaction mixture stirred at 0° C. The mixture was then warmed up to room temperature and stirred for 1.5 hr. The mixture was concentrated to dryness and the crude redissolved in toluene (80 mL). The reaction mixture was heated at 115° C. for 24 hr. The mixture was concentrated to dryness and triturated from methanol to afford 7-fluoro-1-(2-fluoro-phenyl)-3-methyl-1H-quinolin-4-one (1.20 g, 37.8%) as a white solid.

후처리

  1. temperatureThe mixture was then warmed up to room temperature
  2. stirringstirred for 1.5 hr
  3. concentrationThe mixture was concentrated to dryness
  4. dissolutionthe crude redissolved in toluene (80 mL)
  5. temperatureThe reaction mixture was heated at 115° C. for 24 hr
  6. concentrationThe mixture was concentrated to dryness
  7. customtriturated from methanol

출처 및 근거

ORD 기록
ord-a0bc12d08c404f2e8f9f3c2436828414
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501732B2

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