HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichlorobenzaldehyde → HCID 19871210, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichlorobenzaldehyde | HCID 35745 | — |
| Reactant | Methyl 3-aminocrotonate | HCID 643918 | — |
| Reactant | HCID 19871201 | HCID 19871201 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 19871210 | HCID 19871210 | 52.9% |
Reaction Steps
A mixture of 2,3-dichlorobenzaldehyde, 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 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 90°-93° C. (sintering). Yield 52.9%. IR(KBr)cm-1 : 3340, 1695. NMR(CDCl3) δ: 2.28(6H,s, ##STR24## 3.57(3H,s,COOCH3), 4.12(2H,t,J=6,--COOCH2CH2 --), 4.16(1H,s,>N--CH<), 5.42(1H,s,C(4) --H), 5.70(1H,broad s, NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892875 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-f10eced2146d4fd2a05b61cd95be04cf |
| Source note | uspto-grants-1990_01 |