HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 4-(Phenylsulfanyl)-6-ethyl-5-fluoropyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Chloro-6-ethyl-5-fluoropyrimidine | HCID 16743445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Phenylsulfanyl)-6-ethyl-5-fluoropyrimidine | HCID 67542101 | 95% |
Reaction Steps
40 g of 4-chloro-6-ethyl-5-fluoropyrimidine was added to 400 ml of acetonitrile, and 28 ml of thiophenol was added thereto, followed by lowering the temperature to 10° C. 43.39 ml of diisopropylethylamine was added to the resulting solution, and reacted for 2 hours while maintaining the temperature at room temperature. 65 ml of dichloromethane and 200 ml of water were added to the resulting mixture to separate layer, and the resulting aqueous mixture was extracted with 200 ml of dichloromethane. The organic layer was dried over magnesium sulfate and concentrated under a reduced pressure to obtain the title compound as an oil (63.6 g, yield: 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08263769B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-52519844df134ab7b07fa71a8309cc65 |
| Source note | uspto-grants-2012_09 |