HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101351Generated: October 28, 2026
Potassium Carbonate → HCID 57799437, compound
https://huagongshe.com/reaction/2101351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chlorophenylboronic acid | HCID 74299 | — |
| Reactant | HCID 57799433 | HCID 57799433 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57799437 | HCID 57799437 | 75.1% |
Reaction Steps
To a degassed mixture of crude 7-bromo-2-(methoxymethyl)-8-(pyridin-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one (620 mg, 1.85 mmol), 4-chlorophenylboronic acid (850 mg, 5.55 mmol) and K2CO3 (1.02 g, 7.4 mmol) in 1,4-dioxane (18 mL) and H2O (6.0 mL) under argon at 20° C. was added Pd(PPh3)4 (107 mg, 0.093 mmol). The reaction mixture was refluxed for 15 h under argon and then cooled to 20° C. The reaction mixture was diluted with H2O (30 mL) and extracted with EtOAc (3×50 mL). The combined organic extract was washed with saturated aqueous NaHCO3 solution (20 mL), then brine (20 mL), dried over MgSO4, filtered and concentrated in vacuo. The crude product was purified by silica gel column chromatography eluting with a 0-60% gradient of EtOAc in hexanes to obtain the title compound as a yellow solid (510 mg, 1.39 mmol). MS: [M+H]+=367.1. 1H NMR (400 MHz, CDCl3) δ 3.46 (s, 3H), 5.32 (s, 2H), 6.62 (d, J=7.1 Hz 1H), 7.01-7.09 (m, 2H), 7.17-7.22 (m, 2H), 7.23-7.29 (m, 2H), 7.85 (d, J=7.1 Hz, 1H), 8.55 (d, J=4.40 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572808B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-a2d15cef2e5440d6a21a6d233995a5e1 |
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| Source note | uspto-grants-2009_08 |
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