HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 20148554, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 54461528 | HCID 54461528 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20148554 | HCID 20148554 | 60% |
Reaction Steps
A mixture of the product from Step A (10.75 g, 0.038 mol) and 50 ml of acetic anhydride was heated at reflux for 16 hours. After removal of the acetic anhydride in vacuo, the residue was heated in 6 N hydrochloric acid (50 ml) for 3 hours. The cooled reaction mixture was diluted with water (400 ml), chilled and the resulting solid was filtered, washed with water and dried, 5.25 g (60% yield). Recrystallization from water gave 2-sulfamoylthieno[2,3-b]pyridin-6(7H)-one; m.p. 306°-308° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04731368 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-353eaf0330a24f47abe83109a90eed8a |
| Source note | uspto-grants-1988_03 |