HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → HCID 19871249, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | 2-Butenoic acid, 3-amino-, ethyl ester, (2Z)- | HCID 643756 | — |
| Reactant | HCID 19871204 | HCID 19871204 | — |
| Product | HCID 19871249 | HCID 19871249 | 50.8% |
Reaction Steps
A mixture of m-nitrobenzaldehyde, 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 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 82°-85° C. (sintering). Yield 50.8%. IR(Nujol)cm-1 : 3330, 1685. NMR(CDCl3) δ: 1.19(3H,t,J=7,--CH2CH3), 2.26(6H,s, ##STR40## 2.33(6H,s, ##STR41## 4.05(2H,q,J=7,--CH2CH3), 4.10(1H,s,>N--CH<), 4.12(2H,t,J=6,--COOCH2CH2 --), 5.07(1H,s,C(4) --H), 5.75(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-19b2815bf99e4c0c87ff59ada4419f9f |
| Source note | uspto-grants-1990_01 |