HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069891Generated: October 25, 2026
Potassium Carbonate → 4-(2-Butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine
https://huagongshe.com/reaction/2069891
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Butyn-1-ol | HCID 12991 | — |
| Reactant | 4,6-Difluoropyrimidine | HCID 137717 | — |
| Reactant | 3-(Trifluoromethyl)pyrrolidine | HCID 5152159 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-(2-Butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine | HCID 57672951 | — |
Reaction Steps
To a mixture obtained by adding 110.0 g of 4,6-difluoropyrimidine, 132.3 g of potassium carbonate and 19.2 g of triethylamine to 220.0 g of toluene, 69.8 g of 2-butyn-1-ol is added dropwise at 25 to 30° C. over one hour, followed by stirring at 30° C. Then, 220.0 g of water is added dropwise into the reaction mixture, followed by stirring. Then, 152.4 g of 3-trifluoromethylpyrrolidine is added dropwise and, after the mixture is stirred at 30° C., the reaction mixture is allowed to stand. After separating into the organic layer and the aqueous layer, the aqueous layer is removed and the organic layer is washed once with 220.0 g of 5% hydrochloric acid and then washed once with 220.0 g of water. The organic layer is concentrated to obtain 4-(2-butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine (hereinafter referred to as the present compound (2)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08299245B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-7e674331cfe14eaaafee9cbb79f9b92b |
|---|
| Source note | uspto-grants-2012_10 |
|---|