HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → HCID 19871231, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Methyl 3-aminocrotonate | HCID 643918 | — |
| Reactant | HCID 19871201 | HCID 19871201 | — |
| Product | HCID 19871231 | HCID 19871231 | 33.3% |
Reaction Steps
A mixture of m-nitrobenzaldehyde, 2-[4-(4,4'-difluorobenzhydryl)-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'-difluorobenzhydryl)-1-piperazinyl]ethyl methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 68°-72° C. (sintering). Yield 33.3%. This product was treated with methanolic hydrogen chloride to give colorless prisms of the dihydrochloride, m.p. 190°-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892875 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-617ab15aab76475ea097460b20ca7200 |
| Source note | uspto-grants-1990_01 |