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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335269Generated: October 27, 2026

2-Methylpentane → 7-Bromo-N-(2-methyl-5-(2-(4-methylpiperazin-1-yl)benzylcarbamoyl)phenyl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/335269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpentaneHCID 7892—
Reactant2-(4-Methyl-1-piperazinyl)benzenemethanamineHCID 2795568—
ReactantMethyl 3-(7-bromoimidazo[1,2-a]pyridine-3-carboxamido)-4-methylbenzoateHCID 71283103—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product7-Bromo-N-(2-methyl-5-(2-(4-methylpiperazin-1-yl)benzylcarbamoyl)phenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 71283107—

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl 3-(7-bromoimidazo[1,2-a]pyridine-3-carboxamido)-4-methylbenzoate (Intermediate 1B) (400 mg, 1.030 mmol) and TBD (143 mg, 1.030 mmol) in toluene (10 ml) was treated with (2-(4-methylpiperazin-1-yl)phenyl)methanamine (212 mg, 1.030 mmol) and heated at 100° C. under nitrogen overnight. Further TBD (106 mg, 0.82 mmol) was added the mixture was heated at 100° C. for a further 24 hrs. The solvent was removed in vacuo and the residue was partitioned between EtOAc (50 ml) and sodium bicarbonate solution (50 ml). The organic portion was separated and washed with sodium bicarbonate (2×25 ml), dried (MgSO4), filtered and evaporated to dryness to give a yellow solid. Purification by chromatography on silica eluting with 0-20% 2M NH3 in MeOH/DCM afforded a colourless oil. The oil was dissolved in minimum volume of EtOAc and titurated iso-hexane to afford the title compound as a white solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883819B2
Source datasetuspto-grants-2014_11
ORD IDord-4fe692db07194191a3b9e2b5dc83a22a
Source noteuspto-grants-2014_11