HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-bromo-6-(4'-cyclohexylbenzyloxy)-3-ethyl-2-methylthio-4(3H)-pyrimidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Chloromethyl)-4-cyclohexylbenzene | HCID 13343365 | — |
| Reactant | 5-bromo-3-ethyl-6-hydroxy-2-methylthio-4(3H)-pyrimidinone | HCID 136035417 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-bromo-6-(4'-cyclohexylbenzyloxy)-3-ethyl-2-methylthio-4(3H)-pyrimidinone | HCID 14276182 | 100% |
Reaction Steps
In 20 ml of N,N-dimethylformamide were dissolved 1 g of 5-bromo-3-ethyl-6-hydroxy-2-methylthio-4(3H)-pyrimidinone and 0.8 g of 4-cyclohexylbenzyl chloride, and then 1 g of anhydrous potassium carbonate was added thereto. The mixture was subjected to a reaction at 80° C. for 3 hours. After allowing to cool in air, the resulting solution was poured into 50 ml of water and extracted twice with 30 ml of ethyl ether. The ethyl ether layer was washed with water, dried over anhydrous sodium sulfate and then freed of solvent by distillation under reduced pressure to give 1.65 g of a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04908379 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-327ddeef711c4e229ac43d89120d90bf |
| Source note | uspto-grants-1990_03 |