HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057028Generated: November 2, 2026
Potassium Carbonate → 2-((6-methyl-4-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)amino)isonicotinonitrile
https://huagongshe.com/reaction/1057028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methylboronic Acid | HCID 139377 | — |
| Reactant | 2-((6-chloro-4-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)amino)isonicotinonitrile | HCID 72550713 | — |
| Catalyst | HCID 178477754 | HCID 178477754 | — |
| Product | 2-((6-methyl-4-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)amino)isonicotinonitrile | HCID 72550714 | 9% |
Reaction Steps
A vial was charged with 2-[(6-chloro-4-tetrahydropyran-4-yl-2-pyridyl)amino]pyridine-4-carbonitrile (51.1 mg, 0.162 mmol), [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (13.5 mg, 10 mol %), methylboronic acid (20.0 mg, 0.325 mmol), and potassium carbonate (68 mg, 0.49 mmol) and purged under nitrogen before the addition of degassed 1,4-dioxane (1.6 mL) and degassed water (0.5 mL). The mixture was stirred at 100° C. for 19 hr and then diluted with CH2Cl2, filtered through Celite and washed with brine. The organics were dried over MgSO4 and concentrated to dryness. The reaction residue thus obtained was purified by RPLC to afford 2-((6-methyl-4-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)amino)isonicotinonitrile as a white solid (4.1 mg, 9%); ESI-LRMS m/z [M+1]+=295.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09399636B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-f8571fe90a7e4f1ebacfd68d05be7f97 |
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| Source note | uspto-grants-2016_07 |
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