HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Sulfametrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-4-methoxy-1,2,5-thiadiazole | HCID 18177248 | — |
| Solvent | Water | HCID 962 | — |
| Product | Sulfametrole | HCID 64939 | 94.7% |
Reaction Steps
150.6 g of 3-methoxy-4-chloro-1,2,5-thiadiazole (1 mole) were suspended in 156.26 g of dimethyl sulfoxide (2 mole) and 258.31 g of sulfanilamide (1.5 mole) and 414.63 g of potassium carbonate (3 mole) were then added. The mixture was kept at 70° C. for 48 hours while stirring. 600 ml of water were then added, the mixture was cooled to ambient temperature and adjusted to pH 1.5 with concentrated hydrochloric acid. The precipitated crystallized material was filtered off, washed with water and dried. A yield of 271.1 g of crude 3-methoxy-4-(4'-aminobenzenesulfonamido)-1,2,5-thiadiazole (94.67% of theory), melting point 138°-146° C., was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04151164 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-465fd41c1f3c446db97935adfb6ccdaa |
| Source note | uspto-grants-1979_04 |