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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69305Generated: October 29, 2026

Ethyl Acetate → HCID 57917251, compound

https://huagongshe.com/reaction/69305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant3-Tolylboronic acidHCID 2733950—
Reactant(Rac)-6-chloro-3-(1-imidazo[1,2-a]pyridin-6-yl-ethyl)-imidazo[1,2-b]pyridazineHCID 57917275—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 57917251HCID 57917251—

Reaction Conditions

Temperature150 °C

Reaction Steps

(rac)-6-Chloro-3-(1-imidazo[1,2-a]pyridin-6-yl-ethyl)-imidazo[1,2-b]pyridazine (Example 292, 200 mg, 0.672 mmol) was dissolved in DME (3.36 mL) with 3-tolylboronic acid (91 mg, 0.672 mmol), 2 M Na2CO3 solution (1.21 mL, 2.418 mmol) and tetrakis(triphenylphosphine)palladium (38.8 mg, 0.034 mmol). The RM was heated at 150° C. 5 min under microwave irradiations. It was taken up with EtOAc and washed with 10% Na2CO3 solution and brine. Then it was dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography (CombiFlash® Companion System®, with RediSep® silica gel column, 0 to 20% MeOH in DCM). Combined fractions were concentrated. The white solid obtained was a repurified by preparative HPLC with acetonitrile and water (+0.1% TFA). The fractions were joined and were lyophilized. The residue was dissolved in MeOH and it was passed through an SPE cartridge of HCO3− to remove the TFA salt. The filtrate was evaporated to give the free salt of the title compound as a white solid (tR 0.9 min (conditions 2), MH+=354).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-e4c4beaf3ed64d64a6628ae40fdec07d
Source noteuspto-grants-2014_09