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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175165Generated: October 29, 2026

Potassium Carbonate → (S)-3-[1-(1,4-Dimethyl-1H-indol-3-ylmethyl)-5-methyl-2-oxo-1,2-dihydro-imidazo[4,5-b]pyridin-3-yl]-hexanoic acid ethyl ester

https://huagongshe.com/reaction/2175165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant((1,4-Dimethylindole-3-yl)methyl)trimethylammonium iodideHCID 17836486—
Reactant(S)-3-(5-Methyl-2-oxo-1,2-dihydro-imidazo[4,5-b]pyridin-3-yl)-hexanoic acid ethyl esterHCID 58497440—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(S)-3-[1-(1,4-Dimethyl-1H-indol-3-ylmethyl)-5-methyl-2-oxo-1,2-dihydro-imidazo[4,5-b]pyridin-3-yl]-hexanoic acid ethyl esterHCID 5849742245%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of (S)-3-(5-methyl-2-oxo-1,2-dihydro-imidazo[4,5-b]pyridin-3-yl)-hexanoic acid ethyl ester (247 mg, 0.85 mmol) in DMF (5 mL) were added K2CO3 (234 mg, 1.7 mmol) and (1,4-dimethyl-1H-indol-3-ylmethyl)-trimethyl-ammonium iodide (438 mg, 1.27 mmol). The reaction mixture was heated to 60° C. for 48 hours. The reaction mixture was diluted with ethyl acetate and washed with water (×4). The organic phase was dried over Na2SO4 and concentrated. The resulting residue was purified by silica gel preparative TLC using 98:2 CH2Cl2:MeOH as an eluent to afford 170 mg (45%) of the title compound. LCMS, M++1, m/z: 449.47.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062056B2
Source datasetuspto-grants-2015_06
ORD IDord-9ec4544fc6064629b8b01bccc0b9201b
Source noteuspto-grants-2015_06