Methyl chloroformate → Linezolid impurity 3

HRID 1583081

반응식

HRID 1583081 반응식
[F:1][C:2]1[CH:3]=[C:4]([N+:9]([O-])=O)[CH:5]=[CH:6][C:7]=1F.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.O.C(O)(=O)CC(CC(O)=O)(C(O)=O)O.[H][H].C(=O)([O-])[O-].[K+].[K+].Cl[C:41]([O:43][CH3:44])=[O:42]>C1COCC1.O.[Pd].CCCCCCC>[C:41]([NH:9][C:4]1[CH:5]=[CH:6][C:7]([N:12]2[CH2:17][CH2:16][O:15][CH2:14][CH2:13]2)=[C:2]([F:1])[CH:3]=1)([O:43][CH3:44])=[O:42]

참가 물질

11

반응물 6

HCID 6586Methyl chloroformateHCID 8083MorpholineHCID 11430Potassium CarbonateHCID 222302-Hydroxy-1,2,3-propanetricarboxylic acid hydrate (1:1)HCID 1230531,2-Difluoro-4-nitrobenzeneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 10944967Linezolid impurity 3

시약·촉매·용매 4

HCID 23938Palladium촉매HCID 962Water용매2회HCID 8028Tetrahydrofuran용매HCID 8900Heptane용매

실험 절차

3,4-Difluoronitrobenzene (PREPARATION 1, 24.967 g, 156.94 mmol) is added to a mixture of morpholine (60.0 ml, 688 mmol, 4.38 eq) in THF (30 ml) at −6°. The mixture is permitted to warm to 10° over 2 hrs then maintained at 10° for ½ hr. A mixture of citric acid monohydrate (75 g, 357 mmol, 2.27 eq) in water (365 ml) is added with concomitant exotherm to 28°. The phases are separated and the aqueous washed with toluene (95 ml). The organic phases are washed with water (315 ml), the aqueous back wash extracted with toluene (95 ml) and concentrated under reduced pressure. Toluene (76 ml) and methanol (60 ml) are added followed by palladium on carbon (5%, 50% water wet, 3.1370 g, 0.7371 mmol, 0.00470 eq) and the mixture sealed in a Parr shaker. Hydrogen pressure (40 PSI) is applied and maintained while agitating for 4.5 hrs. The catalyst is then removed by filtration under reduced pressure and washed with toluene (100 ml). The mixture is cooled to 2° and a mixte of aqueous potassium carbonate (47%, 17.1 ml, 85 mmol, 0.54 eq) and water (150 ml) is added. Methyl chloroformate (16.4 ml, 212 mmol, 1.35 eq) is then added while maintaining the temperature at about 3-3.5°. The resultant slurry is permitted to warm to 20-25° and stirred 17 hrs. The mixture is warmed to 75° to give a solution, then cooled to 46°, heptane (333 ml) added, then the mixture cooled to 0°, the precipitate collected by filtration with reduced pressure, washed with heptane (100 ml cooled to 5°) then water (230 ml cooled to 5°) and dried to give the title compound, TLC (silica gel; methanol/methylene chloride, 5/95) Rf=0.74 (one spot); NMR (CDCl3) 3.03, 3.76, 3.86, 6.75, 6.87, 6.98, 7.27; CMR (CDCl3) 51.18, 52.42, 67.03, 107.81, 114.56, 119.00, 133.25, 135.77, 154.07, 155.70,

후처리

  1. temperatureto warm to 10° over 2 hrs
  2. temperaturethen maintained at 10° for ½ hr
  3. additionis added with concomitant exotherm to 28°
  4. customThe phases are separated
  5. washthe aqueous washed with toluene (95 ml)
  6. washThe organic phases are washed with water (315 ml)
  7. washthe aqueous back wash
  8. extractionextracted with toluene (95 ml)
  9. concentrationconcentrated under reduced pressure
  10. additionToluene (76 ml) and methanol (60 ml) are added
  11. customthe mixture sealed in a Parr shaker
  12. temperaturemaintained
  13. customThe catalyst is then removed by filtration under reduced pressure
  14. washwashed with toluene (100 ml)
  15. temperatureThe mixture is cooled to 2°
  16. temperaturewhile maintaining the temperature at about 3-3.5°
  17. temperatureto warm to 20-25°
  18. stirringstirred 17 hrs
  19. temperatureThe mixture is warmed to 75°
  20. customto give a solution
  21. temperaturecooled to 46°
  22. temperaturethe mixture cooled to 0°
  23. filtrationthe precipitate collected by filtration with reduced pressure
  24. washwashed with heptane (100 ml cooled to 5°)
  25. dry with materialwater (230 ml cooled to 5°) and dried

출처 및 근거

ORD 기록
ord-0e135bd9a40c4bb78b03f0f97e8da104
출처 데이터셋
uspto-grants-2004_05
특허 번호
US06740754B2

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