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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732469Generated: October 31, 2026

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

https://huagongshe.com/reaction/1732469

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, 0.59 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 numberUS04237300
Source datasetuspto-grants-1980_12
ORD IDord-3ba35ae5428540a995267e874931f0f0
Source noteuspto-grants-1980_12