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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107338Generated: October 25, 2026

m-Chloroperbenzoic acid → 2-[2-(N-isobutyl-N-methylamino)benzylsulfinyl]imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/2107338

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-[2-(N-isobutyl-N-methylamino)benzylthio]imidazo[4,5-b]pyridineHCID 14839445—
SolventChloroformHCID 6212—
Product2-[2-(N-isobutyl-N-methylamino)benzylsulfinyl]imidazo[4,5-b]pyridineHCID 14839446—

Reaction Steps

2-Mercaptoimidazo[4,5-b]pyridine and 2-(N-isobutyl-N-methylamino)benzyl chloride hydrochloride were reacted in an aqueous ethanol solution in the presence of sodium hydroxide to obtain 2-[2-(N-isobutyl-N-methylamino)benzylthio]imidazo[4,5-b]pyridine in the same manner as in Example 1-(2). The obtained 2-[2-(N-isobutyl-N-methylamino)benzylthio]imidazo[4,5-b]pyridine was oxidized by m-chloroperbenzoic acid in chloroform in the same manner as in Example 9-(3) to give 2-[2-(N-isobutyl-N-methylamino)benzylsulfinyl]imidazo[4,5-b]pyridine as a pale yellow crystalline product. m.p.: 116°-118° C. (decompn.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933458
Source datasetuspto-grants-1990_06
ORD IDord-3895279db0d24f64a20273b46b40ecd0
Source noteuspto-grants-1990_06