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 l three-neck round-bottom flask. The internal temperature rose to 30° C. during this, and a solution was produced. After the addition of methanesulfonic acid was complete, the reaction mixture was filtered into a second 1 l three-neck round-bottom flask. The filter was washed with 85 ml of methanol, and the combined filtrates were stirred for 5 h. After the end 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 | US06500830B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-ea4e2ce0abaa47c0beb6e41e12af3ae1 |
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| Source note | uspto-grants-2002_12 |
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