HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 3-chloro-2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole | HCID 72703662 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-chloro-2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole | HCID 72703860 | 100.8% |
Reaction Steps
A mixture of 226 mg of 2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole, 86 mg of N-chlorosuccinimide and 2 ml of DMF was stirred at room temperature for 10 hours. A 10% aqueous sodium thiosulfate solution was poured to the reaction mixture, and the mixture was extracted with t-butyl methyl ether. The organic layer was washed with water and dried over anhydrous magnesium sulfate, then concentrated under reduced pressure. The resulting residue was washed with n-hexane to obtain 250 mg of 3-chloro-2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole (hereinafter, referred to as Compound of Present Invention 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09271500B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-3888f7a4df22403fadecfbef95e3f411 |
| Source note | uspto-grants-2016_03 |