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

HRID 1842448
ノート
印刷プレビュー

反応式

HRID 1842448 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-cd8835e4f1404c92a536a5a59bd06f23
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08946223B2

反応ノート

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