Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Doxazosin | HCID 3157 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Doxazosin Mesylate | HCID 62978 | 163.1% |
Reaction Steps
14.1 g of anhydrous methanesulfonic acid were added to a stirred mixture of 63.2 g of doxazosin, 125 ml of N-methyl-2-pyrrolidone and 500 ml of methanol in a 1 1 three-necked round-bottomed flask. During this time the internal temperature rose to 30° C., and a solution formed. After the addition of the methanesulfonic acid was complete, the reaction mixture was filtered into a second 1 1 three-necked round-bottomed flask. The filter was washed with 85 ml of methanol, and the combined filtrates were stirred for 5 h. After completion of the stirring time, the resulting precipitate was filtered off with suction and washed 3× with 25 ml of methanol each time. 125 g of moist doxazosin mesylate (modification D) were obtained. This corresponds to 70.4 g of dry substance and a yield of 91.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476033B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-4efc50acdf4f4936b08c97e91de74653 |
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| Source note | uspto-grants-2002_11 |
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