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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067026Generated: November 2, 2026

Potassium Phosphate, Tribasic → 8-(4-Bromo-2-chloro-phenylamino)-imidazo[1,5-a]pyridine-7-carboxylic acid methyl ester

https://huagongshe.com/reaction/2067026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Bromo-2-chloroanilineHCID 610169—
Reactant2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
ReactantMethyl 8-chloroimidazo[1,5-a]pyridine-7-carboxylateHCID 59565199—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product8-(4-Bromo-2-chloro-phenylamino)-imidazo[1,5-a]pyridine-7-carboxylic acid methyl esterHCID 5956521350%

Reaction Conditions

Temperature110 °C

Reaction Steps

A suspension of 8-chloro-imidazo[1,5-a]pyridine-7-carboxylic acid methyl ester (300 mg, 1.43 mmol), 4-bromo-2-chloroaniline (354 mg, 1.72 mmol), Pd2dba3 (65 mg, 0.07 mmol), 2-dicyclohexylphosphino-2′,6′-diisopropoxybiphenyl (131 mg, 0.28 mmol) and K3PO4 (424 mg, 2.00 mmol) in toluene (5 ml) was degassed and then heated at 110° 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 and brine, then 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. The resultant residue was subjected to flash chromatography (Si-PPC, gradient 0% to 100%, ethyl actetate in DCM) to afford the title compound as a yellow oil (271 mg, 50%). LCMS (method B): RT=3.65 min, [M+H]+=381/383.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293763B2
Source datasetuspto-grants-2012_10
ORD IDord-1af585ebf4b54b31aeb5f21a83039607
Source noteuspto-grants-2012_10