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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497320Generated: October 30, 2026

Potassium Phosphate, Tribasic → HCID 60209896, compound

https://huagongshe.com/reaction/1497320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant(6-Chloropyridin-3-yl)methanolHCID 177161—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 60209896HCID 60209896—

Reaction Conditions

Temperature140 °C

Reaction Steps

In a microwave vial containing (6-chloropyridin-3-yl)methanol (H1) (0.25 g, 1.7 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazole (63 mg, 0.30 mmol), Pd2(dba)3 (16 mg, 0.02 mmol), and tricyclohexylphosphine (12 mg, 0.04 mmol) was added 7.0 mL of dioxane and 2.3 mL 1.7 M aqueous tribasic potassium phosphate. The reaction was heated to 140° C. in a microwave reactor for 1.5 h. The reaction mixture was extracted with ethyl acetate, dried over sodium sulfate, filtered, and concentrated. The resultant residue was subjected to silica gel chromatography eluting with 0-15% methanol in methylene chloride to afford [6-(1-methyl-1H-pyrazol-4-yl)pyridin-3-yl]methanol (H2) that gave a mass ion (ES+) of 190.2 for M+H+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199939B2
Source datasetuspto-grants-2015_12
ORD IDord-c0f87483b7f1454abaa52cb9ec55b9d9
Source noteuspto-grants-2015_12