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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384134Generated: November 1, 2026

m-Chloroperbenzoic acid → 1-(4-Chloroanilino)-4-(4-pyridylmethyl)phthalazine-3-oxide

https://huagongshe.com/reaction/1384134

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantVatalanibHCID 151194—
ReactantSodium BicarbonateHCID 516892—
SolventAcetateHCID 175—
Product1-(4-Chloroanilino)-4-(4-pyridylmethyl)phthalazine-3-oxideHCID 22741979—

Reaction Steps

A mixture of 1.53 g (4.41 mmol) 1-(4-chloroanilino)-4-(4-pyridylmethyl)phthalazine (see Example 4), 1.74 g (about 5.75 mmol) 3-chloroperbenzoic acid (about 57%), and 80 ml acetate is stirred for 1 h at RT. Then 25 ml 1N aqueous sodium hydrogen carbonate solution is added to the reaction mixture, which is stirred for 10 min, filtered, washed with water, then acetate, and the filter residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm, using an acetate/methanol mixture (19:1). Title compound is obtained after evaporation of the product-containing fractions under vacuum and recrystallization of the filter residue from methanol; m.p. 226-228 0C; ESI-MS: (M+H)+-=363.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258812B1
Source datasetuspto-grants-2001_07
ORD IDord-a60099173aa244a4969b2f1fb5f320f2
Source noteuspto-grants-2001_07