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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081757Generated: November 3, 2026

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

https://huagongshe.com/reaction/1081757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMorpholineHCID 8083—
Reactant5-[2-(Isopropyloxycarbonylamino)ethylthio]imidazo[1,2-a]pyridineHCID 23362812—
SolventAcetic AcidHCID 176—
Product5-[2-(Isopropyloxycarbonylamino)ethylthio]-3-morpholinomethylimidazo[1,2-a]pyridineHCID 2336283550.1%

Reaction Steps

To a solution of an aqueous 37% formalin solution (210 mg, 2.59 mmoles) in acetic acid (2 ml) was added morpholine (226 μl, 2.59 mmoles) under ice-cooling and the mixture was stirred at room temperature for 45 minutes. 5-[2-(isopropyloxycarbonylamino)ethylthio]imidazo[1,2-a]pyridine (651 mg, 2.33 mmoles) was added, followed by stirring at 60° C. for 2 hours. After the solvent was distilled off, the residue was diluted with chloroform, washed in turn with aqueous 1N NaOH and saturated saline, and then dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography [eluent: ethanol/ethyl acetate=1:10] to obtain 442 mg of the desired product (50.1%, light brown solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-aceb1454d68d4045a684024308409f1a
Source noteuspto-grants-1996_12