Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413434Generated: November 1, 2026

m-Chloroperbenzoic acid → 3-Bromo-2-(methoxycarbonylamino)-6-phenylsulfinyl imidazo [1,2-a] pyridine

https://huagongshe.com/reaction/1413434

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-Bromo-2(methoxycarbonylamino)-6(phenylthio) imidazo [1,2-a] pyridineHCID 54463151—
SolventDichloromethaneHCID 6344—
Product3-Bromo-2-(methoxycarbonylamino)-6-phenylsulfinyl imidazo [1,2-a] pyridineHCID 53810012—

Reaction Steps

Alternatively, one may treat a suspension of 3-bromo-2(methoxycarbonylamino)-6(phenylthio) imidazo [1,2-a] pyridine (1.0 gm. 2.64 mmoles) in 100 ml. of dichloromethane with 85% metachloroperbenzoic acid (464 mg., 2.64 mmoles). After 1 hour at room temperature, the solution is washed with aqueous saturated sodium bicarbonate solution, and with water. After drying the solvent is removed in vacuo and the residue is chromatographed over silica gel to yield 3-bromo-2-(methoxycarbonylamino)-6-phenylsulfinyl imidazo [1,2-a] pyridine m.p. 150°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04250174
Source datasetuspto-grants-1981_02
ORD IDord-9b47318919064db39001fc0a3072aa2a
Source noteuspto-grants-1981_02