HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172830Generated: October 31, 2026
Pseudosaccharin chloride → 3-[(1,1-Dioxido-1,2-benzisothiazol-3-YL)amino]-2-thioxo-1,3-thiazolidin-4-one
https://huagongshe.com/reaction/2172830
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pseudosaccharin chloride | HCID 64783 | — |
| Reactant | 3-Aminorhodanine | HCID 74033 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-[(1,1-Dioxido-1,2-benzisothiazol-3-YL)amino]-2-thioxo-1,3-thiazolidin-4-one | HCID 4683478 | 60.8% |
Reaction Steps
To a solution of o-sulfobenzimide (5.00 g) in dioxane (20 ml) were added thionyl chloride (7.5 ml) and dimethylformamide (0.25 ml), and the mixture was stirred overnight at 110° C. The reaction mixture was concentrated under reduced pressure, and to the residue was added toluene (20 ml) to give 3-chloro-1,2-benzisothiazole 1,1-dioxide (3.77 g) as crystals. The obtained 3-chloro-1,2-benzisothiazole 1,1-dioxide (3.77 g) was dissolved in dioxane (20 ml), 3-aminorhodanine (2.77 g) was added thereto, and the mixture was stirred at 110° C. for 1 hr. The reaction mixture was concentrated under reduced pressure, and to the residue was added chloroform (20 ml) to give 3-[(4-oxo-2-thioxothiazolidin-3-yl)amino]-1,2-benzisothiazole 1,1-dioxide (3.56 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09056862B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-a0e0025a28a142179f6c5a4e43c3521e |
|---|
| Source note | uspto-grants-2015_06 |
|---|