HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Phenyl 4-(trifluoromethyl)pyrimidin-2-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 2-Amino-4-(trifluoromethyl)pyrimidine | HCID 595915 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenyl 4-(trifluoromethyl)pyrimidin-2-ylcarbamate | HCID 23212816 | — |
Reaction Steps
According to the procedure described in Example 113B, to a solution of 4-(trifluoromethyl)pyrimidin-2-amine (500 mg, 3.1 mmoles) in 20 mL of tetrahydrofuran was added potassium carbonate (533 mg, 4 mmoles) followed by phenyl chloroformate (626 mg, 4 mmoles). The mixture was stirred at room temperature overnight. After 24 hours, and additional portion of phenyl chloroformate was added and the reaction heated to 60° C. for 3 days. This solution was concentrated to dryness and purified by silica chromatography (eluted with a gradient of 0-5% ethyl acetate/dichloromethane) to afford phenyl 4-(trifluoromethyl)pyrimidin-2-ylcarbamate. 1H NMR (300 MHz, DMSO-d6) δ 11.50 (s, 1H), 9.05 (s, 1H), 7.69 (m, 1H), 7.46 (m, 2H), 7.25 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09320739B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-c3a7976c779145788ce873006f4732ec |
| Source note | uspto-grants-2016_04 |