HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 19365590, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 22397238 | HCID 22397238 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 19365590 | HCID 19365590 | — |
Reaction Steps
To a solution of 4,7-Dihydro-5-carbamoyl-4-oxothieno[2,3-b]pyridine derivative (vih) in an appropriate solvent, e.g. toluene, tetrahydrofuran, dioxane, an equivalent amount or a small excess amount of thioamide reagent, e.g. Lawessons reagent, is added under room temperature or ice-cooling. The mixture is stirred at a temperature of 0° C. to 80° C., and subjected to refluxing under heating if required, to give a 4,7-dihydro-5-thiocarbamoyl-4-oxothieno[2,3-b]pyridine derivative (viih).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05977132 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-6d2f7a13fdd24184af00691dceafdc19 |
| Source note | uspto-grants-1999_11 |