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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081712Generated: October 26, 2026

Formaldehyde → 5-[2-(Methylsulfonylamino)ethylthio]3-morpholinomethylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMorpholineHCID 8083—
Reactant5-[2-(Methylsulfonylamino)ethylthio]imidazo[1,2-a]pyridineHCID 15229363—
SolventAcetic AcidHCID 176—
Product5-[2-(Methylsulfonylamino)ethylthio]3-morpholinomethylimidazo[1,2-a]pyridineHCID 2336285171.5%

Reaction Steps

To a solution of 37% formalin (178 mg, 2.2 mmoles) in acetic acid (2 ml) was added morpholin (192 μl, 2.2 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. 5-[2-(methylsulfonylamino)ethylthio]imidazo[1,2-a]pyridine (543 mg, 2 mmoles) was added to the reaction mixture, followed by stirring at 60° C. for 2 hours. After the solvent was distilled off, the residue was dissolved in chloroform (50 ml) and washed with 1N NaOH (10 ml). Then, the aqueous layer was extracted with chloroform (30 ml×3) and the combined chloroform layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10→1:5) to obtain 530 mg of the desired product (71.5%, colorless solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-e05830de9ec74d43a4d9eff74eb3a55f
Source noteuspto-grants-1996_12