HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-formylbenzoate → HCID 70351527, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-formylbenzoate | HCID 639145 | — |
| Reactant | 2-Butenoic acid, 3-amino-, ethyl ester, (2Z)- | HCID 643756 | — |
| Reactant | HCID 19871204 | HCID 19871204 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 70351527 | HCID 70351527 | 47.5% |
Reaction Steps
A mixture of m-methoxycarbonylbenzaldehyde, 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 ethy 4-(3-methoxycarbonylphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 80°-83° C. (sintering). Yield 47.5%. IR(Nujol)cm-1 : 3330, 1720, 1690. NMR(CDCl3) δ: 1.17(3H,t,J=7,--CH2CH3), 2.25(6H,s, ##STR49## 2.31(6H,s, ##STR50## 3.83(3H,s,--COOCH3), 4.03(2H, q,J=7,--CH2CH3), 4.10(1H,s,>N--CH<), 4.10(2H,t,J=6, --COOCH2CH2 --), 5.00(1H,s,C(4) --H), 5.78(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-27cd96607b9c416dabb5d2655fd50f8f |
| Source note | uspto-grants-1990_01 |