HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 14422496, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19380134 | HCID 19380134 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14422496 | HCID 14422496 | — |
Reaction Steps
60% oily sodium hydride (2.0 g) is suspended in 20 ml of dimethylformamide. A solution of 3.7 ml of ethylmercaptan dissolved in 10 ml of dimethylformamide under ice cooling is added to the suspension below 10° C. and stirred for 30 minutes at room temperature. 2-Chloro-5,7-dimethylpyrazolo [1,5-a]pyrimidine (6.6 g) is added to the mixture and stirred for 5 hours at 80°-90° C. After cooling, the reaction solution is poured into ice water and extracted with toluene. The extract is washed with water and then distilled to remove the solvent. The residue is purified by silica gel chromatography (eluent: dichloromethane) to give 4.0 g of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05017212 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-e00b5538b0194805a1e599e27619a699 |
| Source note | uspto-grants-1991_05 |