HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Sulfamoyl-6-carbamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | 2-Sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine | HCID 20148589 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Sulfamoyl-6-carbamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine | HCID 20148590 | 95% |
Reaction Steps
To a warm (40° C.) solution of 2-sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine (1.42 g, 6.5 mmol) in acetonitrile (80 ml), under a nitrogen atmosphere, was added trimethylsilyl isocyanate (1.0 ml, 7.4 mmol). This solution was stirred for 19 hours and then methanol (2 ml) was added. After 2 hours the precipitated pure product was collected by filtration (1.62 g, 95% yield); m.p. 205°-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04731368 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-e4bea3d02dc24925b9d6c90d2ba756ea |
| Source note | uspto-grants-1988_03 |