HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Amino-1,3,4-thiadiazole-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetazolamide | HCID 1986 | — |
| Reactant | Acetamide 2-acetylamino-1,3,4-thiadiazole-5-sulfonamide | HCID 67839732 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Amino-1,3,4-thiadiazole-2-sulfonamide | HCID 84724 | 85% |
Reaction Steps
This is prepared by hydrolysis of the acetamide 2-acetylamino-1,3,4-thiadiazole-5-sulfonamide (acetazolamide). A slurry of 0.2 mol of acetazolamide in 600 mL of methanol is treated with 60 mL 12N HCl. This mixture is heated with stirring to reflux for 6 hours. Reaction progress is monitored using liquid chromatography. If reaction is not completed after 6 hours, another 30 mL of 12N HCl is added, and the mixture held at reflux for 2 hours. Methanol is then removed under reduced pressure. Product is recovered after raising the pH of the suspension to 7 by addition of NaOH at 0° C.-4° C., followed by filtration. Yield is between 85% and 98% of theoretical with 99% purity. KI =40 nM.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05055480 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-7d5ec70cfe78484ca6525dac5063a9e7 |
| Source note | uspto-grants-1991_10 |