HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-[(2-chlorophenyl)methylidene]-3-oxobutanoate → Phthalimidoamlodipine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-[(2-chlorophenyl)methylidene]-3-oxobutanoate | HCID 299600 | — |
| Reactant | HCID 11174576 | HCID 11174576 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Phthalimidoamlodipine | HCID 9871958 | 70% |
Reaction Steps
24.0 g (75.4 mmoles) of ethyl 3-amino-4-(2-(phthalimido)ethoxy)crotonate and 18.9 g (79.2 mmoles) of methyl 2-(2-chlorobenzylidene)acetoacetate in 64 ml of ethanol were heated under reflux for 20 hours. The reaction mixture was diluted with 56 ml of ethanol and was cooled to crystallise the product. 14.2 g (yield 70%) of 4-(2-chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-2-(2-phthalimidoethoxy)methyl-1,4-dihydropyridine were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06603006B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-3435c4404c6640cf91f4a87b281daaab |
| Source note | uspto-grants-2003_08 |