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Benzyl Bromide → Ethyl 2-benzyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylate

HRID 1842472
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HRID 1842472 반응식
[O:1]=[C:2]1[NH:7][CH2:6][CH2:5][N:4]2[CH:8]=[C:9]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:10]=[C:3]12.C(=O)([O-])[O-].[Cs+].[Cs+].[CH2:22](Br)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>C(#N)C>[CH2:22]([N:7]1[CH2:6][CH2:5][N:4]2[CH:8]=[C:9]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:10]=[C:3]2[C:2]1=[O:1])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1
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참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 10796Cesium carbonateHCID 57517456Ethyl 1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylate

생성물 1

HCID 58465682Ethyl 2-benzyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylate

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
70 °C

실험 절차

To a solution of ethyl 1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylate (29.8 mg, 0.143 mmol) in acetonitrile (1 mL) was added cesium carbonate (60.6 mg, 0.186 mmol) and benzyl bromide (36.7 mg, 0.215 mmol). The reaction mixture was heated at 70° C. overnight. Upon cooling to room temperature all insolubles were removed by filtration and the solvent evaporated to dryness to afforde crude Intermediate 34.

후처리

  1. temperatureUpon cooling to room temperature all insolubles
  2. customwere removed by filtration
  3. customthe solvent evaporated to dryness

출처 및 근거

ORD 기록
ord-3ae347480f1a4d2fbe888bedfcdf9c22
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946223B2

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