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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500681Generated: November 2, 2026

2-(4-Bromo-2-fluorophenylamino)-6-formylaminomethylnicotinic acid methyl ester → 5-(4-Bromo-2-fluorophenylamino)-imidazo[1,5-a]pyridine-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/1500681

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Bromo-2-fluorophenylamino)-6-formylaminomethylnicotinic acid methyl esterHCID 59140162—
ReactantHCID 178479711HCID 178479711—
SolventTolueneHCID 1140—
Product5-(4-Bromo-2-fluorophenylamino)-imidazo[1,5-a]pyridine-6-carboxylic acid methyl esterHCID 5914015349%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of 2-(4-Bromo-2-fluorophenylamino)-6-formylaminomethylnicotinic acid methyl ester (11.8 g, 30.9 mmol) in toluene (550 mL) was added phosphorous (V) oxychloride (3.16 mL, 34 mmol) and the reaction mixture heated at 95° C. for 1 hour. The reaction mixture was concentrated in vacuo and treated with aqueous saturated sodium hydrogen carbonate solution then extracted twice with ethyl acetate. The combined organic fractions were washed with brine, dried (Na2SO4) and concentrated in vacuo. The resultant residue was subjected to flash chromatography (Si-PPC, gradient 0-30% ethyl acetate in DCM) to yield the title compound as a brown oil (5.4 g, 49%). LCMS (Method B): RT=3.56 min, M+H+=364/366.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206174B2
Source datasetuspto-grants-2015_12
ORD IDord-8762685b39e5427c876f4711fd08e141
Source noteuspto-grants-2015_12