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Phosphorus oxychloride → 3-chloro-1-(4-fluorophenyl)pyrazin-2(1H)-one

HRID 1676399
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HRID 1676399 반응식
O=P(Cl)(Cl)[Cl:3].[F:6][C:7]1[CH:12]=[CH:11][C:10]([N:13]2[CH:18]=[CH:17][N:16]=[C:15](OC)[C:14]2=[O:21])=[CH:9][CH:8]=1>CN(C=O)C>[Cl:3][C:15]1[C:14](=[O:21])[N:13]([C:10]2[CH:11]=[CH:12][C:7]([F:6])=[CH:8][CH:9]=2)[CH:18]=[CH:17][N:16]=1
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4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 224243451-(4-fluorophenyl)-3-methoxypyrazin-2(1H)-one

생성물 1

HCID 672214163-chloro-1-(4-fluorophenyl)pyrazin-2(1H)-one수율 64%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
0 °C

실험 절차

POCl3 (5.6 mL, 61.3 mmol) was added dropwise to a solution of 1-(4-fluorophenyl)-3-methoxypyrazin-2(1H)-one in DMF (30 mL) with stirring at 0° C. followed by heating at 90° C. for 1.5 hours. The residue was cooled to 0° C., quenched by adding saturated sodium acetate solution, extracted with CH2Cl2, washed with water, dried over MgSO4, and concentrated. The crude was purified by silica gel flash column chromatography (0.7% MeOH in CH2Cl2) to afford 3.52 g (64%) of the desired product. LRMS (ESI pos) m/e 224.9, 227.0 (M+1, Cl pattern). 1H-NMR (400 MHz, CDCl3) δ 7.41 (m, 2H), 7.21 (m, 4H); 19F-NMR (376 MHz, CDCl3) δ −110.9.

후처리

  1. temperatureby heating at 90° C. for 1.5 hours
  2. temperatureThe residue was cooled to 0° C.
  3. customquenched
  4. additionby adding saturated sodium acetate solution
  5. extractionextracted with CH2Cl2
  6. washwashed with water
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated
  9. customThe crude was purified by silica gel flash column chromatography (0.7% MeOH in CH2Cl2)

출처 및 근거

ORD 기록
ord-a0a78b5b22e747f38dafdae4484df8da
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08003662B2

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