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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447605Generated: November 2, 2026

m-Chloroperbenzoic acid → Methyl 6-(phenylsulfinyl)imidazo(1,2-a)pyridine-2-carbamate

https://huagongshe.com/reaction/1447605

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl [6-(phenylsulfanyl)imidazo[1,2-a]pyridin-2-yl]carbamateHCID 12414300—
SolventDichloromethaneHCID 6344—
ProductMethyl 6-(phenylsulfinyl)imidazo(1,2-a)pyridine-2-carbamateHCID 191716—

Reaction Steps

Alternatively, 0.599 g. (0.002 mole) of the product of Example 3 is combined with 0.406 g. (0.002 moles) of metachloroperbenzoic acid (85%) in 300 ml. of methylene chloride and stirred at room temperature overnight. The solution is washed with saturated aqueous sodium bicarbonate and evaporated to dryness affording 0.75 g. of crude product which is recrystallized from methylene chloride affording 2-(methoxycarbonylamino) 6-(phenylsulfinyl) imidazo [1,2-a] pyridine m.p. 247°-248° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04177274
Source datasetuspto-grants-1979_12
ORD IDord-defae46c58974574a3ab55c3235e0339
Source noteuspto-grants-1979_12