HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101373Generated: November 1, 2026
Potassium Carbonate → 7,8-bis(4-chlorophenyl)-2-(3,3,3-triflouropropyl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one
https://huagongshe.com/reaction/2101373
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-1,1,1-trifluoropropane | HCID 2725114 | — |
| Reactant | 7,8-Bis(4-chlorophenyl)[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one | HCID 57799386 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7,8-bis(4-chlorophenyl)-2-(3,3,3-triflouropropyl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one | HCID 57799442 | 58.6% |
Reaction Steps
To a stirring mixture of 7,8-bis(4-chlorophenyl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one (50 mg, 0.14 mmol) and K2CO3 (40 mg, 0.28 mmol) in DMF (0.47 mL) at 20° C. was added 3-bromo-1,1,1-trifluoropropane (50 mg, 0.28 mmol). The resulting reaction mixture was heated at 80° C. for 60 min. Analysis by HPLC/MS indicated that starting material had been consumed. The reaction mixture was brought to room temperature, diluted with water, and extracted twice with diethyl ether. The combined organic extract was washed with saturated aqueous NaHCO3 solution, then brine, then dried (MgSO4), filtered, and concentrated under reduced pressure. The crude product was purified by reverse phase preparative HPLC (acetonitrile-water-TFA) to isolate the title compound (37 mg, 0.082 mmol) as a yellow oil. MS: [M+H]+=452.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07572808B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-9078fafd8c604c259edd997261b6f478 |
|---|
| Source note | uspto-grants-2009_08 |
|---|