HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Thioglycolate → HCID 21241315, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-chloro-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidine | HCID 520127 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21241315 | HCID 21241315 | — |
Reaction Steps
Ethyl thioglycollate, 1.2 g, is dissolved in 30 ml of dry ethanol, to which 400 mg of sodium hydride (60% in an oil) is added under cooling with ice water and stirred for 10 minutes. Then 1.7 g of 7-chloro-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidine and 10 ml of dry dichloromethane are added and stirred for 16 hours. To the reaction mixture, water and dichloromethane are added and the organic layer is separated. The separated organic layer is washed with saline and dried over anhydrous potassium carbonate. The solvent is evaporated under reduced pressure and the residue is purified by column chromatography [on 40 g of silica gel, developed and eluted with ethyl acetate] to give 2.2 g of the desired compound as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04826834 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-3715ae08be1442abba4548a5a4379b28 |
| Source note | uspto-grants-1989_05 |