HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-sulfamoyl-3,4-dihydrothieno[3,2-f]-1,4-thiazepin-5(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cysteamine | HCID 6058 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 2-chloro-5-sulfamoylthiophene-3-carboxylate | HCID 19106450 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-sulfamoyl-3,4-dihydrothieno[3,2-f]-1,4-thiazepin-5(2H)-one | HCID 19106476 | — |
Reaction Steps
To a round bottomed flask were added ethanol (200 mL) followed by solid sodium (1.0 g, 43.5 mmole). After the sodium dissolved, 2-aminoethanethiol was added (1.57 g, 20.4 mmole). The reaction was stirred for approximately 5.0 minutes and 5-chloro-4-carboethoxythiophene-2-sulfonamide (5.0 g, 18.5 mmole) was added. The reaction was heated at reflux for 24 hrs. The cooled reaction mixture was acidified (6.0N HCl) and the solvent was removed under vacuum. The residue was triturated with water and the resulting solid collected: 4.77 g (98%) mp>270° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05276025 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-92ea9783b6a44c5b87d9308cc48e1c23 |
| Source note | uspto-grants-1994_01 |