HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501251Generated: October 30, 2026
Water → Methyl 4-[4-(4-fluorophenyl)-1,1-dioxoisothiazolidin-2-yl]-5-methanesulfonyl-2-methylbenzoate
https://huagongshe.com/reaction/501251
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Methyl 4-fluoro-5-methanesulfonyl-2-methylbenzoate | HCID 10538364 | — |
| Reactant | 4-(4-Fluorophenyl)-1,2-thiazolidine-1,1-dione | HCID 68463636 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-[4-(4-fluorophenyl)-1,1-dioxoisothiazolidin-2-yl]-5-methanesulfonyl-2-methylbenzoate | HCID 68462085 | 94.8% |
Reaction Steps
18.00 g of 4-(4-fluorophenyl)isothiazolidine 1,1-dioxide, 20.59 g of methyl 4-fluoro-5-methanesulfonyl-2-methylbenzoate (Journal of Medicinal Chemistry (1997), 40(13), 2017) and 81.75 g of Cs2CO3 were stirred in 500 ml of anhydrous DMF at RT for 5 hours. Then a further 2.00 g of methyl 4-fluoro-5-methanesulfonyl-2-methylbenzoate were added, and the mixture was stirred at RT for 1 hour and left to stand at RT for 15 hours. The reaction mixture was poured into 1800 ml of water and stirred at RT for 1 hour, and the product was filtered off with suction. The product was then dissolved in 1 l of EA, and the solution was mixed with MgSO4 and activated carbon and stirred at RT for 15 minutes. It was then filtered and the solvent was removed in vacuo. 35.00 g of a colorless foam were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07772262B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-828a5a89407b409191281d8af3dbcdd4 |
|---|
| Source note | uspto-grants-2010_08 |
|---|