Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetic-formic anhydride | HCID 75269 | — |
| Reactant | HCID 13663190 | HCID 13663190 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86740815 | HCID 86740815 | — |
Reaction Steps
Formic acetic anhydride (15 ml; prepared by heating a mixture of formic acid (5 ml) and acetic anhydride (10 ml) at 50°-60° C. for 1 hour) was added over 10 minutes to a stirred, ice-cooled solution of 2-(2-aminoethoxymethyl)-4-(2,3-dichlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridine (4.4 g) in tetrahydrofuran (30 ml). The mixture was stirred at room temperature for 1.5 hours and then evaporated. The residue was dissolved in dichloromethane and the solution washed with 10% aqueous sodium carbonate solution, dried (Na2SO4), and evaporated. The residual solid was collected, washed with diethyl ether and dried to give the title compound as a hemihydrate (4.0 g), m.p. 178°-181° C. Found: C, 52.69; H, 5.05; N, 6.06. C21H24Cl2N2O6.0.5H2O requires C, 52.51; H, 5.25; N, 5.83%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04590195 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-7eec42167f9444f4b55fa55888221e11 |
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| Source note | uspto-grants-1986_05 |
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