HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → HCID 19871228, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Methyl 3-aminocrotonate | HCID 643918 | — |
| Reactant | HCID 19871203 | HCID 19871203 | — |
| Product | HCID 19871228 | HCID 19871228 | 57.8% |
Reaction Steps
A mixture of m-nitrobenzaldehyde, 2-[4-(4,4'-dichlorobenzhydryl)-1-piperazinyl]ethyl acetoacetate and methyl 3-aminocrotonate was worked up in isopropyl alcohol in the same manner as Example 1 to give 2-[4-(4,4'-dichlorobenzhydryl)-1-piperazinyl]ethyl methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 83°-87° C. (sintering). Yield 57.8%. This product was further treated with ethanolic hydrogen chloride to give the dihydrochloride. Recrystallization from ethanol-ethyl ether gave light yellow prisms, m.p. 208°-211° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892875 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-04d5fb0a79ac41f08bb89d988441cc22 |
| Source note | uspto-grants-1990_01 |