HuagongsheHuagongshe Chemistry Print Report · For research reference only
Amlodipine → HCID 86758618, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Amlodipine | HCID 2162 | — |
| Reactant | Atorvastatin | HCID 60823 | — |
| Reactant | Chloromethyl chloroformate | HCID 62754 | — |
| Reactant | Calcium | HCID 5460341 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86758618 | HCID 86758618 | — |
Reaction Steps
Chloromethyl chloroformate (2.85 g, 22 mmol) is added to amlodipine (10.5 g, 20 mmol) and pyridine (1.6 g) in 300 ml chloroform cooled in an ice bath. The reaction mixture is stirred at room temperature for 16 h, washed with water, dried (anhydrous sodium sulfate) and concentrated under reduced pressure. The residue is dissolved in dimethylformamide (50 ml) containing the calcium salt of atorvastatin (10.75 g, 0.018 mol) and the reaction mixture is heated at 80° C. for 20 h. The dimethylformamide is removed in vacuo and the residue is triturated with chloroform-hexane to yield the title compound the title compound of Example Two.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06486182B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-515c249ab1b544f6b9c2313c5e5ab908 |
| Source note | uspto-grants-2002_11 |