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Potassium Carbonate → 1-(4-fluorophenyl)-3-methoxypyrazin-2(1H)-one

HRID 2241371
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HRID 2241371 반응식
C([O-])([O-])=O.[K+].[K+].Cl[C:8]1[N:9]=[C:10]([O:22][CH3:23])[C:11](=[O:21])[N:12]([C:14]2[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=2)[CH:13]=1>CO.[Pd]>[F:20][C:17]1[CH:16]=[CH:15][C:14]([N:12]2[CH:13]=[CH:8][N:9]=[C:10]([O:22][CH3:23])[C:11]2=[O:21])=[CH:19][CH:18]=1
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참가 물질

5

반응물 2

HCID 11430Potassium CarbonateHCID 673472395-chloro-1-(4-fluorophenyl)-3-methoxypyrazin-2(1H)-one

생성물 1

HCID 224243451-(4-fluorophenyl)-3-methoxypyrazin-2(1H)-one수율 90%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

K2CO3 (1.09 g, 7.85 mmol) and 10% Pd/C (0.42 g, 0.39 mmol) were added to 5-chloro-1-(4-fluorophenyl)-3-methoxypyrazin-2(1H)-one (2.0 g, 7.85 mmol) in MeOH (100 mL) at room temperature under a H2 atmosphere and the reaction was stirred for 6 hours. The reaction mixture was filtered with MeOH and concentrated under reduced pressure. The crude was treated with CH2Cl2, washed with water, dried over MgSO4, and concentrated to give the desired product (1.55 g, 90%). LRMS (ESI pos) m/e 221.0 (M+1).

후처리

  1. filtrationThe reaction mixture was filtered with MeOH
  2. concentrationconcentrated under reduced pressure
  3. additionThe crude was treated with CH2Cl2
  4. washwashed with water
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-d3fb530f86a9449aab13af856901e781
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07723330B2

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