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Potassium Carbonate → HCID 90410457, 화합물

HRID 1527751
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HRID 1527751 반응식
F[C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][C:15]=1[N+:16]([O-:18])=[O:17])[O:5][CH2:6][C:7]1[CH:11]=[CH:10][N:9]([CH3:12])[N:8]=1.C([O-])([O-])=O.[K+].[K+].[CH3:25][C:26]1[CH:31]=[C:30]([O:32][C:33]([F:36])([F:35])[F:34])[CH:29]=[CH:28][C:27]=1[CH2:37][NH2:38]>C(#N)C>[CH3:12][N:9]1[CH:10]=[CH:11][C:7]([CH2:6][O:5][C:4]2[CH:13]=[CH:14][C:15]([N+:16]([O-:18])=[O:17])=[C:2]([CH:3]=2)[NH:38][CH2:37][C:27]2[CH:28]=[CH:29][C:30]([O:32][C:33]([F:34])([F:35])[F:36])=[CH:31][C:26]=2[CH3:25])=[N:8]1
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 577941232-Methyl-4-(trifluoromethoxy)benzylamineHCID 828819703-((3-Fluoro-4-nitrophenoxy)methyl)-1-methyl-1H-pyrazole

생성물 1

HCID 90410457HCID 90410457, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
90 °C

실험 절차

To a solution of 3-((3-fluoro-4-nitrophenoxy)methyl)-1-methyl-1H-pyrazole (143 mg, 0.573 mmol) in acetonitrile (10 mL) was added K2CO3 (317 mg, 2.3 mmol) followed by (2-methyl-4-(trifluoromethoxy)phenyl)methanamine (117 mg, 0.573 mmol). The mixture was stirred at 90° Celsius overnight. The reaction was cooled to RT and concentrated to dryness. The resulting residue was dissolved in DCM (50 mL) and washed with water (50 mL). The organic phase was concentrated to give the title compound. MS (ESI): mass calcd. for C20H19F3N4O4, 436.14; m/z found, 437 [M+H]+.

후처리

  1. temperatureThe reaction was cooled to RT
  2. concentrationconcentrated to dryness
  3. dissolutionThe resulting residue was dissolved in DCM (50 mL)
  4. washwashed with water (50 mL)
  5. concentrationThe organic phase was concentrated

출처 및 근거

ORD 기록
ord-0fbef858a0634cc7881ad70b9ca93086
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09089569B2

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