Sulfuric Acid → Clopidogrel bisulfate
Reaction equation
[CH3:1][O:2][C:3]([C@@H:5]([N:13]1[CH2:21][C:17]2[CH:18]=[CH:19][S:20][C:16]=2[CH2:15][CH2:14]1)[C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][C:11]=1[Cl:12])=[O:4].[S:22](=[O:26])(=[O:25])([OH:24])[OH:23]>C(O)(C)C>[CH3:1][O:2][C:3]([C@@H:5]([N:13]1[CH2:21][C:17]2[CH:18]=[CH:19][S:20][C:16]=2[CH2:15][CH2:14]1)[C:6]1[C:11]([Cl:12])=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:4].[OH:25][S:22]([OH:26])(=[O:24])=[O:23]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Clopidogrel base (2.89 g) was dissolved in isopropanol (44 mL). Eighty percent aqueous sulfuric acid (0.42 mL) was added to the solution at 20° C. The reaction mixture was heated to reflux temperature for 2 hours. The solution was cooled to room temperature and stirred at this temperature for an additional 5 hours. Then half of the solvent was removed by evaporation under reduced pressure and the resulting solution was stored at room temperature for 45 minutes to obtain a white precipitate. The solid was collected by filtration, washed with IPA (3×10 ml) and dried at 50° C. in a vacuum oven for 15 hours to obtain 1.24 g (33%) of clopidogrel hydrogensulfate crystal Form IV.
Workup
- temperatureThe reaction mixture was heated
- temperatureto reflux temperature for 2 hours
- customThen half of the solvent was removed by evaporation under reduced pressure
- waitthe resulting solution was stored at room temperature for 45 minutes
- customto obtain a white precipitate
- filtrationThe solid was collected by filtration
- washwashed with IPA (3×10 ml)
- customdried at 50° C. in a vacuum oven for 15 hours
Sources & evidence
- ORD record
- ord-54d89a4f8a55464d88343966b45eea5b
- Source dataset
- uspto-grants-2006_07
- Patent number
- US07074928B2
Reaction notes
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