HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011245Generated: October 31, 2026
Potassium Carbonate → HCID 24946129, compound
https://huagongshe.com/reaction/1011245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-Aminocarbonylphenylboronic acid | HCID 2737811 | — |
| Reactant | HCID 57664375 | HCID 57664375 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 24946129 | HCID 24946129 | 42.2% |
Reaction Steps
To a reaction vial (40 mL), is added 5-chloro-N-(4-(4-propylpiperazin-1-yl)phenyl)-[1,2,4]triazolo[1,5-a]pyridin-8-amine (55 mg, 0.15 mmol), potassium carbonate (104 mg, 0.75 mmol, 5 eq.), 4-carbamoylphenylboronic acid (50 mg, 0.30 mmol, 2 eq), PddppfCl2 (20 mg, 15%), dioxane (4.0 mL) and water (1.0 mL). The reaction mixture is degassed and filled with argon. The reaction is heated at 105-110° C. for 20 h. After cooling to rt, ethyl acetate (10 mL) is added to each reaction vial. The organic phase was filtered through a pat of celite and then is evaporated to give a dry residue that was purified by preparatory HPLC to give the title compound, 28.9 mg, yield 42.2%; LCMS-ESI (m/z): calcd for C26H29N7O, 455; [M+H]+ found, 456.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07977352B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-1751fa034b814cd1a72240a6e37fb267 |
|---|
| Source note | uspto-grants-2011_07 |
|---|