HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromopinacolone → HCID 21392477, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromopinacolone | HCID 21642 | — |
| Reactant | 4-prop-2-enylpiperazine-1-carbothioamide | HCID 4740506 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21392477 | HCID 21392477 | — |
Reaction Steps
3.7 g of 4-allyl-1-piperazinyl-thiocarboxamide are added to a solution of 3.6 g of bromopinacoline in 40 cc of ethanol, and the reaction mixture is subsequently heated to the boil at reflux for 2 hours. The mixture is subsequently concentrated by evaporation in a vacuum, the residue is dissolved in a small amount of water and divided between ether and a concentrated aqueous sodium hydroxide solution. The ether phase is washed with water, dried over sodium sulphate and saturated with hydrogen chloride gas after filtration. The monohydrochloride of 2-(4-allyl-1-piperazinyl)-4-tert.butyl-thiazole crystallizes and has an M.P. of 212°-214° after recrystallization from ethanol/diisopropyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064244 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-aeffb55f95fd41658204d7f3c3b97d7a |
| Source note | uspto-grants-1977_12 |