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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380035Generated: November 2, 2026

Sodium Carbonate → HCID 20692746, compound

https://huagongshe.com/reaction/380035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(1S,2R)-4-(2-hydroxy-1-methyl-4-pyridin-3-ylbutoxy)benzeneboronic acidHCID 54413593—
ReactantHCID 71436066HCID 71436066—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductHCID 20692746HCID 20692746117.9%

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 (0.150 g, Example 33), 3-bromobenzenesulfonic acid, pyrrolidinyl amide (0.290 g), 2M aqueous sodium carbonate (0.50 ml) and tetrakis(triphenylphosphine)palladium(0) (0.025 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 a gum, which was further purified by reverse-phase HPLC to give the title compound as a foam (0.137 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300352B1
Source datasetuspto-grants-2001_10
ORD IDord-a496955efd834e3fb4de5c61311ce277
Source noteuspto-grants-2001_10