HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Tebatizole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-Chloropinacolone | HCID 83572 | — |
| Reactant | 4-Methylpiperazine-1-carbothioamide | HCID 2113086 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Tebatizole | HCID 3085056 | — |
Reaction Steps
1.34 g of chloropinacoline are dissolved in 15 cc of absolute ethanol. After the addition of 1.6 g of 4-methyl-1-piperazinyl-thiocarboxamide, the mixture is heated to the boil on a water bath for 1 hour. Cooling is then effected and diethyl ether is added until the mixture remains turbid. The precipitated crystals are filtered off and recrystallized from ethanol. The resulting 2-(4-methyl-1-piperazinyl)-4-tert.butyl-thiazole hydrochloride has an M.P. of 206°. The base liberated from its hydrochloride in known manner by treatment with an aqueous sodium hydroxide solution has a B.P. of 97°-99°/0.2 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064244 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-4fbe36d5628d44b490376f262fb0ccdf |
| Source note | uspto-grants-1977_12 |