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Potassium Carbonate → Ethyl 1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylate

HRID 1842448
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HRID 1842448 반응식
[N:1]([CH2:4][CH2:5][N:6]1[CH:10]=[C:9]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:8]=[C:7]1[C:16]([O:18]CC)=O)=[N+]=[N-].C(=O)([O-])[O-].[K+].[K+]>CCO.[Pd]>[O:18]=[C:16]1[NH:1][CH2:4][CH2:5][N:6]2[CH:10]=[C:9]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:8]=[C:7]12
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참가 물질

5

반응물 2

HCID 11430Potassium CarbonateHCID 57517455diethyl 1-(2-azidoethyl)-1H-pyrrole-2,4-dicarboxylate

생성물 1

HCID 57517456Ethyl 1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylate수율 41%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a solution of diethyl 1-(2-azidoethyl)-1H-pyrrole-2,4-dicarboxylate (10 g, 35.68 mmol) in EtOH (1000 mL) was added 10% Pd/C (3 g). The resulting residue was stirred at rt under a 30 psi H2 atmosphere for 2 h. The palladium catalyst was filtered. To the filtrate was added potassium carbonate (5 g, 36 mmol) and the mixture was refluxed overnight. All solids were removed by filtration, and the filtrate was concentrated. Purification via flash chromatography (DCM: methanol, 50:1 to 20:1) afforded ethyl 1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylate (2.5 g, 41%). 1H NMR (DMSO-d6, 300 MHz) δ7.91 (s, 1 H), 7.64 (s, 1H), 6.90 (s, 1 H), 4.18 (m, 4 H), 3.50 (m, 2 H), 1.25 (t, J=5.4 Hz, 3 H).

후처리

  1. filtrationThe palladium catalyst was filtered
  2. temperaturethe mixture was refluxed overnight
  3. customAll solids were removed by filtration
  4. concentrationthe filtrate was concentrated
  5. customPurification via flash chromatography (DCM: methanol, 50:1 to 20:1)

출처 및 근거

ORD 기록
ord-cd8835e4f1404c92a536a5a59bd06f23
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946223B2

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