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Potassium Carbonate → 2-[5-(2-Cyano-4-fluorophenoxy)-indazol-1-yl]-N,N-dimethylacetamide

HRID 2112207
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HRID 2112207 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[NH:16][N:15]=[CH:14]3)=[C:6]([CH:9]=1)[C:7]#[N:8].Cl[CH2:21][C:22]([N:24]([CH3:26])[CH3:25])=[O:23].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C.[I-].C([N+](CCCC)(CCCC)CCCC)CCC>[C:7]([C:6]1[CH:9]=[C:2]([F:1])[CH:3]=[CH:4][C:5]=1[O:10][C:11]1[CH:12]=[C:13]2[C:17](=[CH:18][CH:19]=1)[N:16]([CH2:21][C:22]([N:24]([CH3:26])[CH3:25])=[O:23])[N:15]=[CH:14]2)#[N:8]
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참가 물질

6

반응물 3

HCID 11430Potassium CarbonateHCID 758862-chloro-N,N-dimethylacetamideHCID 574187532-(1H-Indazol-5-yloxy)-5-fluorobenzonitrile

생성물 1

HCID 674094872-[5-(2-Cyano-4-fluorophenoxy)-indazol-1-yl]-N,N-dimethylacetamide수율 12%

시약·촉매·용매 2

HCID 67553Tetrabutylammonium Iodide촉매
HCID 6228
Dimethylformamide
용매

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온도
110 °C

실험 절차

To a solution of 5-fluoro-2-(1H-indazol-5-yloxy)-benzonitrile (44d) (0.200 g, 0.790 mmol) in DMF (6 mL) was added 2-chloro-N,N-dimethylacetamide (0.115 g, 0.948 mmol) and tetrabutyl ammonium iodide (0.088 g, 0.237 mmol), followed by K2CO3 (0.164 g, 1.19 mmol). The mixture was heated to 110° C. for 48 hours under N2 atmosphere. The reaction mixture was concentrated under reduced pressure and dissolved in dichloromethane. The solution was washed with 1N HCl, filtered, and chromatographed on Biotage eluting with 5% MeOH in dichloromethane to afford 0.032 g of the product (12% yield).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. dissolutiondissolved in dichloromethane
  3. washThe solution was washed with 1N HCl
  4. filtrationfiltered
  5. customchromatographed on Biotage
  6. washeluting with 5% MeOH in dichloromethane

출처 및 근거

ORD 기록
ord-62fca6a811e2449097821f9781327c1a
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07521447B2

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