HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → N-benzyl-4-(3-chloro-4-methoxybenzyloxy)-2-(methylsulfinyl) pyrimidine-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | N-benzyl-4-(3-chloro-4-methoxybenzyloxy)-2-(methylmercapto)pyrimidine-5-carboxamide | HCID 71235045 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-benzyl-4-(3-chloro-4-methoxybenzyloxy)-2-(methylsulfinyl) pyrimidine-5-carboxamide | HCID 71235049 | — |
Reaction Steps
N-benzyl-4-(3-chloro-4-methoxybenzyloxy)-2-(methylmercapto)pyrimidine-5-carboxamide (100 mg, 0.23 mmol) was dissolved in 10 mL of dichloromethane, m-CPBA (m-chloroperbenzoic acid, 40 mg, 0.23 mmol) was added and reacted at room temperature for 3 h, washed with water after the reaction is complete, extracted with dichloromethane, the organic layer was dried and dried by rotation to obtain yellow solid, and this product was directly used in the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08980904B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-0b78f2baa56a4aa6b5eef5f7768aa3fb |
| Source note | uspto-grants-2015_03 |