Phosphorus oxychloride → Ethyl 6-chloro-2-(2,4-difluorophenyl)pyridine-3-carboxylate

HRID 1257092노트

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HRID 1257092 반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:13][CH:12]=[CH:11][N+:10]=1[O-].P(Cl)(Cl)([Cl:23])=O>ClC(Cl)C>[Cl:23][C:11]1[CH:12]=[CH:13][C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[C:9]([C:3]2[CH:4]=[CH:5][C:6]([F:8])=[CH:7][C:2]=2[F:1])[N:10]=1

참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 582235643-Pyridinecarboxylic acid, 2-(2,4-difluorophenyl)-, ethyl ester, 1-oxide2회

생성물 1

HCID 21062879Ethyl 6-chloro-2-(2,4-difluorophenyl)pyridine-3-carboxylate

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매

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온도
72.5 °C

실험 절차

To a nitrogen purged 500 mL, 3-necked flask, fitted with a reflux condenser, heating mantle and a thermocouple was charged 2-(2,4-difluorophenyl)-3-(ethoxycarbonyl)pyridine 1-oxide, 4 (21 g, 75 mmoles, 1.0 eq), followed by 150 mL dichloroethane. Phosphorous oxychloride (75 mL) was added in one aliquate with stirring, causing an immediate rise in temperature from 21 to 23° C. followed by gradual warming. The solution was heated under nitrogen to 70-75° C. (completeness of reaction determined by HPLC). The reaction was then cooled to room temperature and concentrated under vacuum to remove most of the POCl3. The remainder was quenched by slowly pouring onto 450 g of ice. The mixture (after the ice melted) was then extracted into methylene chloride (2×200 mL). The combined organics were dried (MgSO4), filtered through silica, eluted with methylene chloride, and concentrated to give the title Compound, 5, as an orange solid. 1H NMR (500.0 MHz, CDCl3) d 8.15 (d, J=8.2 Hz, 1H), 7.54 (td, J=8.5, 5.0 Hz, 1H), 7.34 (d, J=8.2 Hz, 1H), 6.96-6.92 (m, 1H), 6.79-6.74 (m, 1H), 4.16 (q, J=7.2 Hz, 2H), 1.10 (t, J=7.1 Hz, H) ppm.

후처리

  1. customTo a nitrogen purged 500 mL, 3-necked flask
  2. customfitted with a reflux condenser
  3. temperatureheating mantle
  4. customfrom 21 to 23° C.
  5. custom(completeness of reaction determined by HPLC)
  6. temperatureThe reaction was then cooled to room temperature
  7. concentrationconcentrated under vacuum
  8. customto remove most of the POCl3
  9. customThe remainder was quenched
  10. additionby slowly pouring onto 450 g of ice
  11. extractionwas then extracted into methylene chloride (2×200 mL)
  12. dry with materialThe combined organics were dried (MgSO4)
  13. filtrationfiltered through silica
  14. washeluted with methylene chloride
  15. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8e5f0261278d45dbb5c5807affb603bd
출처 데이터셋
uspto-grants-2013_06
특허 번호
US08461345B2

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