HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 2-(2-Ethylsulfonylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 118205820 | HCID 118205820 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(2-Ethylsulfonylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidine | HCID 118205815 | — |
Reaction Steps
60 mg of 3-chloroperbenzoic acid (purity of 65% or more) was added to a mixture of 40 mg of 2-(2-ethylsulfanylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidine and 3 ml of chloroform, under ice cooling, and the mixture was stirred at room temperature for 4 hours. A 10% aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to obtain 44 mg of 2-(2-ethylsulfonylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidine (Compound of Present Invention 19).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328121B1 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-b26e3732f41245198526ba8a0258c2cc |
| Source note | uspto-grants-2016_05 |