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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107340Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 14839450, compound

https://huagongshe.com/reaction/2107340

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 14839449HCID 14839449—
SolventChloroformHCID 6212—
ProductHCID 14839450HCID 14839450—

Reaction Steps

2-Mercaptoimidazo[4,5-b]pyridine and 2-(N-cylopentylamino)benzyl chloride hydrochloride were reacted in an aqueous ethanol solution to obtain 2-[2-(N-cyclopentylamino)benzylthio[-imidazo[4,5-b]pyridine in the same manner as in Example 9-(2). The obtained 2-[2-(N-cyclopentylamino)benzylthio]imidazo[4,5-b]pyridine was oxidized by m-chloroperbenzoic acid in chloroform in the same manner in Example 9-(3) to give 2-[2-(N-cyclopentylamino)benzylsulfinyl]imidazo[4,5-b]pyridine as a pale yellow crystalline product. m.p.: 134° C. (decompn.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933458
Source datasetuspto-grants-1990_06
ORD IDord-09ac4084f1cd40c990c2a968069889a4
Source noteuspto-grants-1990_06