HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichlorobenzaldehyde → HCID 19871227, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichlorobenzaldehyde | HCID 35745 | — |
| Reactant | 2-Butenoic acid, 3-amino-, ethyl ester, (2Z)- | HCID 643756 | — |
| Reactant | HCID 19871204 | HCID 19871204 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 19871227 | HCID 19871227 | 27.3% |
Reaction Steps
A mixture of 2,3-dichlorobenzaldehyde, 2-[4-(4,4'-dimethylbenzhydryl)-1-piperazinyl]ethyl acetoacetate and ethyl 3-aminocrotonate was worked up in isopropyl alcohol in the same manner as Example 1 to give 2-[4-(4,4'-dimethylbenzhydryl)-1-piperazinyl]ethyl ethyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 85°-88° C. (sintering). Yield 27.3%. IR(Nujol)cm-1 : 3330, 1690. NMR(CDCl3) δ: 1.14(3H,t,J=7,--CH2CH3), 2.25(12H,s, ##STR37## 4.05(2H,q,J=7,--CH2CH3), 4.08(1H,s,>N--CH<), 4.08(2H,t, J=6,--COOCH2CH2 --), 5.41(1H,s,C(4) --H), 5.68(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-0a5715abcc0644c6b124525d80488494 |
| Source note | uspto-grants-1990_01 |