Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109040Generated: October 26, 2026

Hydrochloric Acid → HCID 178426582, compound

https://huagongshe.com/reaction/2109040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Amino-5-methylpyridineHCID 15348—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178499199HCID 178499199—
SolventChloroformHCID 6212—
ProductHCID 178426582HCID 17842658261.6%

Reaction Steps

2-Amino-5-methylpyridine (81 mg) is dissolved in chloroform (5 ml). After adding 0.98 M trimethyl alminum-hexane solution (763 μl) under ice-cooling, the reaction solution is stirred under ice-cooling for 10 minutes, and then at room temperature for 0.5 hours. To the resulting reaction solution is added methyl 3-({[trans-4-(3-oxomorpholin-4-yl)cyclohexyl]carbonyl}amino)furo[3,2-b]pyridine-2-carboxylate (150 mg) obtained in Reference Example 79, and the mixture is stirred at room temperature for 2 hours and at 50° C. under heating for 5 hours. To the reaction solution is added 10% hydrochloric acid (3 ml) under ice-cooling, and the mixture is stirred at room temperature for 0.5 hours. The reaction solution is then neutralized by adding saturated aqueous sodium hydrogen carbonate solution, and extracted with chloroform. The organic layer is washed with saturated brine, dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by NH-silica gel column chromatography (eluent: ethyl acetate followed by ethyl acetate/methanol=10/1). The resulting solid is suspended in diethyl ether, and collected by filtration to give the title compound (110 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514449B2
Source datasetuspto-grants-2009_04
ORD IDord-5d4253a68d7e4a83a6d4a5f344be7462
Source noteuspto-grants-2009_04