HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 19835105, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | HCID 19835132 | HCID 19835132 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19835105 | HCID 19835105 | — |
Reaction Steps
15.5 ml (16.5 g) of thiophenol are added to a suspension of 9.35 g of 2-methylsulphinyl-4-amino-5-cyanothiazole, prepared according to example I, in 250 ml of acetonitrile, while stirring. After stirring at room temperature for another 30 minutes and leaving to stand overnight, the mixture is filtered with charcoal, after which the filtrate is evaporated. The residue is taken up in methylene chloride, after which the resulting solution is washed, successively with 2N sodium hydroxide solution and water, dried, filtered and diluted with isopropanol. After evaporating the methylene chloride the desired product crystallises in a yield of 7.62 g; m.p. 176°-18° C.; Rf (CH2Cl2) 0.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04889863 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-a3cb6883f659435cb211d9c0f1990818 |
| Source note | uspto-grants-1989_12 |