Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 19106454 | HCID 19106454 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19106468 | HCID 19106468 | 80% |
Reaction Steps
A suspension of 4-isobutyryl-5(R,S)-methyl-7-sulfamoyl-2,3,4,5-tetrahydrothieno[3,2-f]-1,4-thiazepine-1,1-dioxide (500 mg, 1.5 mmol) in water (8 mL) and concentrated HCl (4 mL) containing ethanol (3 mL) was warmed at 100° C. for 2 days. The cooled solution was made weakly basic with NaHCO3 and the product was extracted into ethyl acetate. The extract was dried (Na2SO4), filtered through a pad of charcoal and the solvent evaporated. Trituration of this residue afforded 361 mg (80%) of title compound, mp 236°-238° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05276025 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-280a2b3960ec465480477d47eed01e21 |
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| Source note | uspto-grants-1994_01 |
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