HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570141Generated: October 27, 2026
Sodium Carbonate → N-{4-[2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]pyridin-2-yl}acetamide
https://huagongshe.com/reaction/570141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-(4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)acetamide | HCID 49760417 | — |
| Reactant | 3-Bromo-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine | HCID 83747438 | — |
| Catalyst | Bis(tricyclohexylphosphine)palladium(II) Dichloride | HCID 11556747 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-{4-[2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]pyridin-2-yl}acetamide | HCID 90387180 | 17% |
Reaction Steps
3-Bromo-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine (150 mg, 0.51 mmol) and N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]acetamide (148 mg, 0.56 mmol, 1.1 eq) are dissolved in 1.5 mL 1,4-dioxan. To this mixture, bis(tricyclohexylphosphine)palladium(II)-dichloride (57 mg, 0.07 mmol, 0.15 eq) and 0.83 mL sodium carbonate solution (2 molar) are added. The reaction mixture is flushed with argon for 5 mins and then sealed. Next the mixture is heated for 30 min at 150° C. in the microwave (Biotage). The reaction mixture is then poured in water and extracted with dichloromethane (3×20 mL). The organic layer is dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material is purified by column chromatography using silica gel in heptane and ethyl acetate (1:0 to 1:1) as eluent and 0.03 g (17%) of N-{4-[2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]pyridin-2-yl}acetamide are obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09023844B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-6fb2e7e00eaa4498aabd96ebb2001015 |
|---|
| Source note | uspto-grants-2015_05 |
|---|