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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250374Generated: October 30, 2026

Sodium Bicarbonate → HCID 178428706, compound

https://huagongshe.com/reaction/2250374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
ReactantN-(2-amino-iodo-pyridin-3-yl)-3-(6-amino-4-methyl-pyridin-2-yl)-propionamideHCID 69198093—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178428706HCID 17842870654.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

96 mg N-(2-amino-iodo-pyridin-3-yl)-3-(6-amino-4-methyl-pyridin-2-yl)-propionamide (compound A10) is dissolved in 3.0 ml anoxic dioxane under a nitrogen atmosphere. Subsequently, 0.7 ml of an aqueous sodium bicarbonate solution (2.0 M), 52 mg 4-(trifluoromethyl)phenyl-boronic acid, and 14 mg trans-dichloro-bis(tricyclohexylphosphane)palladium-(II) are added. The reaction mixture is refluxed at 110° C. for 20 h. Thereafter, the volatile components are removed in vacuo and the remaining residue is re-dissolved in a mixture of water/dichloromethane (1:1). The aqueous phase is extracted several times with dichloromethane. The organic layer is separated, dried using sodium sulfate, and evaporated to dryness to yield 161 mg of a colourless, crude solid. Subsequently, the residue is purified by flash chromatography on silica gel (eluent: dichloromethane/ethanol 8:1) to afford 52 mg of the title compound. M.p. 170° C. ESI-MS: 398.3 (MH+). TLC: Rf=0.25 (dichloromethane/methanol 8:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317021B2
Source datasetuspto-grants-2008_01
ORD IDord-54b5474cb3634ab8846ba97a1824984b
Source noteuspto-grants-2008_01