HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-Piperazinecarboxamide, N-((dimethylamino)carbonyl)-N-methyl-4-(1-methylethyl)-, monohydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 13094265 | HCID 13094265 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Piperazinecarboxamide, N-((dimethylamino)carbonyl)-N-methyl-4-(1-methylethyl)-, monohydrochloride | HCID 3066979 | 65.1% |
Reaction Steps
To 20 ml of ethanol, were added 5.0 g of 1-(2,4,4-trimethylallophanoyl)piperazine hydrochloride and 3.7 g of sodium carbonate. To the resulting mixture, was added dropwise with stirring 2.5 g of isopropyl bromide. The mixture was allowed to react under reflux for 8 hours and the precipitate was removed by filtration. The filtrate was concentrated and the residue was purified with a silica gel column to obtain an oil. This oil was converted to hydrochloride in the customary way and recrystallized from ethanol to obtain 3.8 g (65% yield) of 1-(isopropyl)-4-(2,4,4-trimethylallophanoyl)piperazine hydrochloride having a melting point of 213°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666911 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-a473463f5ffb407abca5674709b84438 |
| Source note | uspto-grants-1987_05 |