HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → HCID 19871229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | Methyl 3-aminocrotonate | HCID 643918 | — |
| Reactant | HCID 19871201 | HCID 19871201 | — |
| Product | HCID 19871229 | HCID 19871229 | 21.3% |
Reaction Steps
A mixture of o-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-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate as a light yellow powder, m.p. 90°-93° C. (sintering). Yield 21.3%. IR(KBr)cm-1 : 3350, 1695. NMR(CDCl3) δ: 2.26(3H,s, ##STR22## 2.31(3H,s, ##STR23## 3.53(3H,s,COOCH3), 4.0-4.3(3H,m,>N--CH<+--COOCH2CH2 --), 5.72(1H,s,C(4) --H), 5.77(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-8fa7c5d18b364dd29dee32823c7e7162 |
| Source note | uspto-grants-1990_01 |