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Ethyl 2-acetyl-3-(dimethylamino)acrylate → Ethyl-2-(4-fluorophenyl)-4-methylpyrimidine-5-carboxylate

HRID 219655
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인쇄 미리보기

반응식

HRID 219655 반응식
Cl.[F:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([NH2:9])=[NH:8])=[CH:5][CH:4]=1.[Na].[CH2:13]([O:15][C:16](=[O:25])[C:17]([C:22](=O)[CH3:23])=[CH:18]N(C)C)[CH3:14]>C(O)C>[CH2:13]([O:15][C:16]([C:17]1[C:22]([CH3:23])=[N:8][C:7]([C:6]2[CH:10]=[CH:11][C:3]([F:2])=[CH:4][CH:5]=2)=[N:9][CH:18]=1)=[O:25])[CH3:14]
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참가 물질

5

반응물 3

HCID 3806790Ethyl 2-acetyl-3-(dimethylamino)acrylateHCID 5360545SodiumHCID 124561604-Fluorobenzamidine Hydrochloride

생성물 1

HCID 69279303Ethyl-2-(4-fluorophenyl)-4-methylpyrimidine-5-carboxylate수율 88.5%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

4-Fluorobenzamidine hydrochloride (1.25 g, 7.16 mmol) is added to a solution of sodium metal (0.17 g, 7.39 mmol) in dry ethanol (25 mL) and stirred at room temperature for 20 min. Ethyl-2-acetyl-3-(dimethylamino)acrylate (1.35 g, 7.16 mmol) is added. The mixture is heated to reflux for 3 hours. The solvent is removed in vacuo. The residue is dissolved in EtOAc, washed with water and brine, dried (MgSO4), filtered and concentrated in vacuo to afford ethyl-2-(4-fluorophenyl)-4-methyl-pyrimidine-5-carboxylate (1.65 g, 87%) as a solid. MS: 261 (M+H) 261.

후처리

  1. temperatureThe mixture is heated
  2. temperatureto reflux for 3 hours
  3. customThe solvent is removed in vacuo
  4. dissolutionThe residue is dissolved in EtOAc
  5. washwashed with water and brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-49464ad095e64e3e876387f003083b10
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08202863B2

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