Sulfuric Acid → Clopidogrel bisulfate

HRID 1792104Notes

Reaction equation

HRID 1792104 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]>C1(C)C=CC=CC=1>[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

HCID 1118Sulfuric AcidHCID 60606Clopidogrel

Product 1

HCID 115366Clopidogrel bisulfateYield 82%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Clopidogrel base (4.29 g, 1 eq.) was dissolved in toluene (33.8 mL). Eighty percent aqueous sulfuric acid (1.04 mL, 1.1 eq.) was added to the solution at 20° C. The reaction mixture was heated to reflux temperature for 3 hours. Then, the solution was cooled to room temperature and stirred at this temperature for an additional 16 hours during which a massive precipitate was formed. The white solid was collected by filtration, washed with toluene (2×10 ml) and dried at 50° C. in a vacuum oven for 24 hours to obtain 4.59 g (82%) of clopidogrel hydrogensulfate crystal Form II.

Workup

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux temperature for 3 hours
  3. customwas formed
  4. filtrationThe white solid was collected by filtration
  5. washwashed with toluene (2×10 ml)
  6. customdried at 50° C. in a vacuum oven for 24 hours

Sources & evidence

ORD record
ord-32168cbcc4634df6ae32c9a9b1ce0afe
Source dataset
uspto-grants-2006_07
Patent number
US07074928B2

Reaction notes

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