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Methyl 2-[(2-chlorophenyl)methylidene]-3-oxobutanoate → Phthalimidoamlodipine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl 2-[(2-chlorophenyl)methylidene]-3-oxobutanoate | HCID 299600 | — |
| 反応物 | HCID 11174576 | HCID 11174576 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Phthalimidoamlodipine | HCID 9871958 | 70% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06603006B2 |
| 出典データセット | uspto-grants-2003_08 |
| ORD ID | ord-3435c4404c6640cf91f4a87b281daaab |
| 出典メモ | uspto-grants-2003_08 |