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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380039Generated: October 29, 2026

Sodium Carbonate → HCID 57047089, compound

https://huagongshe.com/reaction/380039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(1S,2R)-4-(2-hydroxy-1-methyl-4-pyridin-3-ylbutoxy)benzeneboronic acidHCID 54413593—
ReactantHCID 79466300HCID 79466300—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductHCID 57047089HCID 57047089—

Reaction Conditions

Temperature90 °C

Reaction Steps

Prepared according to the method described in Example 12b) from (1S,2R)-4-[2-hydroxy-1-methyl-4-pyridin-3-ylbutoxy]benzeneboronic acid (0.20 g, Example 33 (0.290 g), 3-bromo-4-methylbenzoic acid, methyl amide (0.30 g), 2M aqueous sodium carbonate (0.66 ml) and tetrakis(triphenylphosphine)palladium(0) (0.038 g) in ethanol (3 ml). The reaction mixture was heated at 90° C. for 4 hours. After cooling, the solution was concentrated under reduced pressure, taken up in ethanol and concentrated again (twice). The residue was triturated with acetone and then filtered through silica gel. The filtrate was concentrated under reduced pressure, dissolved in dichloromethane, filtered and purified by normal-phase HPLC eluting with a gradient of 0-25% ethanol in dichloromethane to give an oil, which was further purified by column chromatography over silica gel eluting with ethyl acetate:ethanol (9:1) to give the title compound as a foam(0.20 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300352B1
Source datasetuspto-grants-2001_10
ORD IDord-1e08a867a6cd4981a3f2ae8b8b8e0834
Source noteuspto-grants-2001_10