HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81235Generated: October 30, 2026
Potassium Phosphate, Tribasic → HCID 178435922, compound
https://huagongshe.com/reaction/81235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Phenylvinylboronic acid, pinacol ester | HCID 11031671 | — |
| Reactant | HCID 178461197 | HCID 178461197 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Product | HCID 178435922 | HCID 178435922 | — |
Reaction Steps
A sealed tube was charged with 2-bromo-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile (Preparative Example 3.1, 150 mg, 0.337 mmol), 4,4,5,5-tetramethyl-2-(1-phenylethenyl)-1,3,2-dioxaborolane (93 mg, 0.405 mmol), PdCl2(dppf)-dichloromethane adduct (27.5 mg, 0.034 mmol), and potassium phosphate (215 mg, 1.012 mmol). The tube was evacuated and backfilled with argon (3×). Fully degassed dioxane (1.53 mL) and water (0.153 mL) were added. The vial was sealed and heated at 50° C. overnight. The mixture was then cooled to room temperature and directly purified via silica gel chromatography (0-100% ethyl acetate/hexanes) to afford 4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-(1-phenylethenyl)-3H-imidazo[4,5-c]pyridine-6-carbonitrile as a yellow solid. MS ESI calcd. for C28H26ClN5 [M+H]+ 468. found 468.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846657B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a3a7ec8b04a94bc09bc86b1b6a7ecbef |
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| Source note | uspto-grants-2014_09 |
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