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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067014Generated: October 25, 2026

Potassium Phosphate, Tribasic → HCID 59565225, compound

https://huagongshe.com/reaction/2067014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
Reactant2-Fluoro-4-(methylsulfanyl)anilineHCID 22025617—
ReactantMethyl 8-chloroimidazo[1,5-a]pyridine-7-carboxylateHCID 59565199—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 59565225HCID 5956522539%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 8-chloro-imidazo[1,5-a]pyridine-7-carboxylic acid methyl ester (223 mg, 1.06 mmol), 2-fluoro-4-methylsulfanyl-phenylamine (200 mg, 1.27 mmol), Pd2dba3 (39 mg, 0.04 mmol), 2-dicyclohexylphosphino-2′,6′-diisopropoxybiphenyl (79 mg, 0.17 mmol) and K3PO4 (315 mg, 1.48 mmol) in toluene (4 mL) was degassed and then heated at 100° C. for 18 hours. The reaction mixture was then cooled to room temperature and diluted with ethyl acetate. The resultant mixture was washed with water followed by brine, before being loaded onto a 10 g Isolute® SCX-2 cartridge which was eluted with methanol, and then a 2M solution of ammonia in methanol. The appropriate fractions were combined and concentrated in vacuo to give a residue. The residue was subjected to flash chromatography (Si-PPC, gradient 0% to 10%, ethyl actetate in dichloromethane) to afford the title compound as a yellow oil (136 mg, 39%). LCMS (method B): RT=3.26 min, [M+H]+=332.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293763B2
Source datasetuspto-grants-2012_10
ORD IDord-39ce8e7a203246159a04b80be43208df
Source noteuspto-grants-2012_10