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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505402Generated: October 29, 2026

Sodium Bicarbonate → HCID 178428705, compound

https://huagongshe.com/reaction/505402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantPhenylboronic acid 1,3-propanediol esterHCID 642685—
ReactantHCID 178428704HCID 178428704—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178428705HCID 17842870580.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

350 mg of 2-[2-(amino-4-methylpyridin-6-yl)ethyl]-6-bromo-3H-imidazo[4,5-b]pyridine (compound 4) are dissolved in 5.6 ml of anoxic dioxane under a nitrogen atmosphere. Subsequently, 3.15 ml of an aqueous sodium bicarbonate solution (2.0 M), 193 mg of 2-phenyl-1,3,2-dioxaborinane, and 49 mg of trans-dichloro-bis(tricyclohexylphosphane)palladium-(II) are added. The reaction mixture is refluxed at 110° C. for 46 hours. Thereafter, the volatile components are removed in vacuo and the remaining residue is redissolved in 200 ml of a mixture of water/dichloromethane (1:1). The aqueous phase is extracted twice each with 125 ml of dichloromethane. The organic layer is separated, dried using sodium sulfate, and evaporated to dryness to yield a colorless, crude solid. Subsequently, the residue is purified by flash chromatography on silica gel (eluent: dichloromethane/methanol 8:1) to afford 279 mg of the title compound as a colorless solid of m.p. 230° C. MS: 330.3 (MH+). TLC: Rf=0.34 (dichloromethane/methanol 8:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781453B2
Source datasetuspto-grants-2010_08
ORD IDord-f499970186cc42e583f421d0829cf0fe
Source noteuspto-grants-2010_08