HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46283Generated: October 25, 2026
Hydrochloric Acid → 3-cyano-4-(2-iodo-phenoxy)-N-[1,2,4]thiadiazol-5-yl-benzenesulfonamide
https://huagongshe.com/reaction/46283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Iodophenol | HCID 10784 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-cyano-4-fluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide | HCID 58042302 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-cyano-4-(2-iodo-phenoxy)-N-[1,2,4]thiadiazol-5-yl-benzenesulfonamide | HCID 59436635 | 88.7% |
Reaction Steps
To a solution of 2-iodophenol (6.0 mmol, 1320 mg) and K2CO3 (10.5 mmol, 1450 mg) in DMF (15.0 mL) was added 3-cyano-4-fluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide (Preparation 65, 4.5 mmol, 1280 mg). The reaction mixture was heated at 80° C. for 24 hours. The reaction was cooled to room temperature and the mixture was poured into 1 N aqueous HCl (100 mL) to obtain a white solid. The afforded solid was washed with heptane and the solid was dried in vacuo to furnish 1.932 g of the title compound. LCMS Rt=1.67 minutes MS m/z 485 [MH]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08541588B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-d03a31da76ca4ebf9a89d430e4f66cd3 |
|---|
| Source note | uspto-grants-2013_09 |
|---|