Pamidronic Acid → Pamidronate disodium hydrate

HRID 1862080

Reaction equation

HRID 1862080 reaction equation
[CH2:1]([C:4]([P:10]([O-:13])([OH:12])=[O:11])([P:6]([O-:9])([OH:8])=[O:7])[OH:5])[CH2:2][NH2:3].[Na+:14].[Na+].C(C(P(O)(O)=O)(P(O)(O)=O)[OH:20])CN.[OH-].[Na+]>O>[CH2:1]([C:4]([P:10]([O-:13])([OH:12])=[O:11])([P:6]([O-:8])([OH:9])=[O:7])[OH:5])[CH2:2][NH2:3].[OH2:20].[Na+:14].[Na+:14]

Participants

5

Reactant 3

HCID 4674Pamidronic Acid2×HCID 14798Sodium Hydroxide2×HCID 73351Pamidronate Disodium Anhydrous

Product 1

HCID 16078998Pamidronate disodium hydrate

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

In the process for preparing crystalline disodium pamidronate from the reaction solution for neutralization of pamidronic acid with sodium hydroxide according to the first method, it is characterized to be included the process which pamidronic acid is neutralized with sodium hydroxide at about 90° C. in the range of pH 7.5˜8.5: the insoluble materials produced after neutralization is filtered: an alcohol is added to the filtrate to produce a salt: the resulting salt is dissolved in water and is allowed to stand at room temperature to induce crystallization: the resulting crystallizing solution is cooled to obtain the crystals: and then the resulting crystals are dried at the temperature of 75˜85° C. under normal pressure to obtain the crystalline disodium pamidronate hydrate.

Workup

  1. customthe insoluble materials produced after neutralization
  2. filtrationis filtered
  3. additionan alcohol is added to the filtrate
  4. customto produce a salt
  5. customto stand at room temperature
  6. customcrystallization
  7. customthe resulting crystallizing solution
  8. temperatureis cooled
  9. customto obtain the crystals
  10. customthe resulting crystals are dried at the temperature of 75˜85° C. under normal pressure

Sources & evidence

ORD record
ord-eb517ef6275e4eaeb46cc2131a17235e
Source dataset
uspto-grants-2003_03
Patent number
US06534674B2

Linked notes

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