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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251494Generated: November 4, 2026

m-Chloroperbenzoic acid → HCID 10595309, compound

https://huagongshe.com/reaction/1251494

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 10641825HCID 10641825—
ReactantDichloromethane methanolHCID 21226129—
SolventChloroformHCID 6212—
ProductHCID 10595309HCID 10595309142%
ProductHCID 10641825HCID 10641825—

Reaction Steps

Part A: A solution of 1.24 g of 1-(2-bromo-4-isopropyl-phenyl)-3-cyano-6-methyl-7-azaindole (Example 72) and 1.42 g of 85% 3-chloro-peroxybenzoic acid in 20 mL of chloroform was refluxed for 6 hrs. The mixture was cooled and washed first with 10% sodium bicarbonate solution, then with brine. The solution was dried (Na2SO4) and evaporated to give a residue. TLC on silica gel with 95:5 dichloromethane-methanol showed a trace spot at Rf 0.88 and a major spot at Rf 0.34. The material was purified by chromatography on silica gel with dichoromethane, followed by 1% methanol in dichloromethane, to give a trace of unchanged 1-(2-bromo-4-isopropylphenyl)-3-cyano-6-methyl-7-azaindole (Rf 0.88) and 0.92 g of 1-(2-bromo-4-isopropylphenyl)-3-cyano-6-methyl-7-azaindole 7-oxide (Rf0.34); mp 179.2°. Mass spec. (m+H)+=370.0559; calcd., 370.0555 (79Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342503B1
Source datasetuspto-grants-2002_01
ORD IDord-b60bc3b2b9224d7981e792f3ddd76cf7
Source noteuspto-grants-2002_01