Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Amlodipine | HCID 2162 | — |
| Reactant | Ethanesulfonic acid | HCID 11668 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86591094 | HCID 86591094 | 90% |
Reaction Steps
Into a 1L three-neck flask, ethanesulfonic acid (11.56 g, 1.05 equivalents) and methanol (200 ml) were poured. To the flask, a solution of amlodipine (40.8 g, 0.1 mole) in methanol (300 ml) was added dropwise. The resulting solution was stirred at 23° C. for 2 hours, cooled to 7° C. and stirred again for 1 hour to produce precipitates. They were washed at 5° C. with methanol (100 ml) and n-hexane (100 ml), filtered, and dried at 35° C. in vacuo to afford 46.4 g of amlodipine ethanesulfonate as a white crystalline solid (Yield 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06903124B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-f493bd9425bf493386f142da8598659b |
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| Source note | uspto-grants-2005_06 |
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