Methane → Zoledronic Acid

HRID 2116816Notes

Reaction equation

HRID 2116816 reaction equation
[N:1]1(C(CC(O)=O)=O)[CH:5]=[CH:4][N:3]=[CH:2]1.[P:12]([OH:15])([OH:14])[OH:13].P(Cl)(Cl)Cl.C.C1([O:27][C:28]2[CH:33]=CC=CC=2)C=CC=CC=1>CO.C1(C)C=CC=CC=1.O>[CH:4]1[N:3]=[CH:2][N:1]([CH2:33][C:28]([P:12]([OH:15])([OH:14])=[O:13])([P:12]([OH:15])([OH:14])=[O:13])[OH:27])[CH:5]=1

Participants

9

Conditions

Temperature
70 °C

Procedure

The suspension of (1-imidazoyl)ethanoic acid (10.0 g) and phosphorous acid (19.5 g) in diphenyl ether (50 ml) was heated up to 70° C. for 1 hour. Phosphorous trichloride (20 ml) was slowly added to reaction mass at 70° C. temperature and maintained reaction temperature for another 6 hours. Reaction mass was cooled to 25° C. followed by addition of water (150 ml) and toluene (30 ml). Reaction mixture was again heated to 70° C. and charged charcoal in hazy biphasic solution, stirred, filtered through Hyflo bed, washed the bed with hot water (30 ml). Layers was separated from filtrate, aqueous layer was washed with toluene (20 ml) and combined organic layer was then back extracted with water (20 ml) and mixed with main aqueous layer. The water (140 ml) was distilled out from combined aqueous layer at atmospheric pressure in 2 hours and then refluxed the concentrated mass for 13 hours. Reaction mass was cooled to 25° C. followed by addition of methanol (50 ml) in 1 hours. The reaction mixture was stirred and again cooled to 0° C. followed filtration. The filtrate was washed with chilled 1:2 mixture (30 ml) of water and methanol and dried at 60° C. to get Zoledronic Acid.

Workup

  1. temperaturemaintained
  2. customreaction temperature for another 6 hours
  3. customReaction mass
  4. temperaturewas cooled to 25° C.
  5. customReaction mixture
  6. temperaturewas again heated to 70° C.
  7. filtrationfiltered through Hyflo bed
  8. washwashed the bed with hot water (30 ml)
  9. customLayers was separated from filtrate, aqueous layer
  10. washwas washed with toluene (20 ml)
  11. extractionwas then back extracted with water (20 ml)
  12. additionmixed with main aqueous layer
  13. distillationThe water (140 ml) was distilled out
  14. customin 2 hours
  15. temperaturerefluxed the concentrated mass for 13 hours
  16. customReaction mass
  17. temperaturewas cooled to 25° C.
  18. stirringThe reaction mixture was stirred
  19. temperatureagain cooled to 0° C.
  20. filtrationfiltration
  21. washThe filtrate was washed
  22. temperaturewith chilled 1:2 mixture (30 ml) of water and methanol
  23. customdried at 60° C.

Sources & evidence

ORD record
ord-208c9159b7594b4592609475978b7503
Source dataset
uspto-grants-2008_10
Patent number
US07439385B2

Reaction notes

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