Ethanol → 827573-11-5
Reaction equation
[OH-].[Na+:2].C(O)C.CO.[CH:8]1[N:12]=[CH:11][N:10]([CH2:13][C:14]([P:20]([OH:23])([OH:22])=[O:21])([P:16]([OH:19])([OH:18])=[O:17])[OH:15])[CH:9]=1>O.CC(O)C>[CH:8]1[N:12]=[CH:11][N:10]([CH2:13][C:14]([P:16]([O-:19])([O-:18])=[O:17])([P:20]([O-:22])([OH:23])=[O:21])[OH:15])[CH:9]=1.[Na+:2].[Na+:2].[Na+:2]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of sodium hydroxide (1.4 g) in a mixture of water (40% v/v)/Ethanol or Methanol or IPA (60% v/v, 10 volumes per grams of ZLD-Ac form XII) (13 ml) was added drop-wise to a suspension of Zoledronic acid form XII (5.0 g) in a mixture of water (40% v/v)/Ethanol or Methanol or IPA (60% v/v, 10 volumes per grams of ZLD-Ac) (71 ml) at reflux temperature. The reaction mixture was heated at reflux temperature for additional 16 hours. Then the reaction mixture was cooled to room temperature. Further cooling was performed using an ice-bath. The precipitate was then filtered, washed and dried in a vacuum oven at 50° C. for 24 hours to give Zoledronate trisodium crystal form IX.
Workup
- additionwas added drop-wise
- temperatureat reflux temperature
- temperatureThe reaction mixture was heated
- temperatureat reflux temperature for additional 16 hours
- temperatureFurther cooling
- filtrationThe precipitate was then filtered
- washwashed
- customdried in a vacuum oven at 50° C. for 24 hours
Sources & evidence
- ORD record
- ord-13bb47e1357b4a96a12211c6d3aa797b
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435827B2
Reaction notes
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