HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(4-Chlorophenyl)-2-furaldehyde → HCID 19375563, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(4-Chlorophenyl)-2-furaldehyde | HCID 676184 | — |
| Reactant | HCID 19375560 | HCID 19375560 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19375563 | HCID 19375563 | — |
Reaction Steps
A solution of 1-amino-3-[4-(4-methyl-1-piperazinyl)butyl]-2,4-imidazolidinedione, hydrochloride (0.0094 mole), dimethylformamide (75 ml) and 5-(4-chlorophenyl)-2-furancarbox aldehyde [prepared as described in U.S. Pat. No. 4,882,354, to Huang et al., assigned to Norwich Eaton Pharmaceuticals, Inc., issued Nov. 21, 1984; see Cols. 7 and 8 hereby incorporated by reference herein] (1.94 g, 0.0094 mole) is stirred at ambient temperature for 72 hours. The mixture is filtered, collecting the solid. Recrystallization from absolute ethanol/H2O and air-drying gives 2.63 g (0.0050 mole) of 1-[[[5-(4-chlorophenyl)-2-furanyl]methylene]amino]3-[4-methyl-1-piperazinyl)butyl]-2,4-imidazolidinedione dihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05462940 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-cbb9b6ecbd2a4d7886ba39ff10a4679f |
| Source note | uspto-grants-1995_10 |