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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917615Generated: November 2, 2026

Sodium Carbonate → HCID 58505685, compound

https://huagongshe.com/reaction/1917615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Pyridinylboronic acidHCID 2734378—
ReactantHCID 58505584HCID 58505584—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58505685HCID 5850568565.6%

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of ethyl 3-{3-[(4-bromophenyl)carbonyl]-1-(2,2-dimethylpropanoyl)-7-(pyridin-2-ylmethoxy)indolizin-2-yl}-2,2-dimethylpropanoate (225 mg, 0.363 mmol), 3-pyridyl boronic acid (89.3, 0.726 mmol), tetrakis(triphenylphosphine)palladium(0) (42.0 mg, 0.036 mmol) in THF (4.0 mL) and aqueous 20% Na2CO3 (2.0 mL) is heated at 70° C. for 24 h then cooled to 23° C. The mixture is partitioned between Et2O and water then the organics are collected, dried with MgSO4, filtered, and concentrated in vacuo. Purification of the crude by flash chromatography (SiO2, hexanes to EtOAc) gives ethyl 3-[1-(2,2-dimethylpropanoyl)-7-(pyridin-2-ylmethoxy)-3-{[4-(pyridin-3-yl)phenyl]carbonyl}indolizin-2-yl]-2,2-dimethylpropanoate (147 mg, 65%) which is dissolved in THF (1.0 mL), MeOH (1.0 mL), and 6M aqueous NaOH (0.8 mL) and heated at 50° C. for 3 h then cooled to 23° C. and acidified to pH=1 with concentrated aqueous HCl. The mixture is concentrated in vacuo, diluted with DMSO, filtered, and filtrate is purified by HPLC (25% CH3CN to 85% CH3CN in 0.1% TFA in water) to give the title compound (62 mg, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618300B2
Source datasetuspto-grants-2013_12
ORD IDord-895d84f68c5743a89f0f2dac59cedcac
Source noteuspto-grants-2013_12