HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-(2-Chlorophenyl)-N-[2-(dimethylamino)ethyl]-1-piperazinecarboxamide, hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 1-(2-Chlorophenyl)piperazine | HCID 415628 | — |
| Reactant | N-[2-(Dimethylamino)ethyl]-4-(4-fluorophenyl)-1-piperazinecarboxamide | HCID 14763463 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 4-(2-Chlorophenyl)-N-[2-(dimethylamino)ethyl]-1-piperazinecarboxamide, hydrochloride | HCID 14763465 | — |
Reaction Steps
This compound was prepared according to the procedure used to synthesize the compound of Example 11. A mixture of 4.9 g (0.03 mole) of 1,1'-carbonyldiimidazole, 2.6 g (0.03 mole) of unsym-diethylethylenediamine, and 5.9 g (0.03 mole) of 1-(2-chlorophenyl)piperazine in a total of 200 ml of tetrahydrofuran gave an oil as residue. The hydrochloride was formed in ethereal hydrogen chloride and the collected solid was recrystallized from methanol-ethyl ether to yield 3.4 g (33%) of title compound as a white solid, m.p. 185°-188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960776 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-14c6b684ff3d4884bb2b57a654a71236 |
| Source note | uspto-grants-1990_10 |