Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057710Generated: October 27, 2026

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

https://huagongshe.com/reaction/1057710

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 1 N aqueous sodium hydrogencarbonate 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° C.; ESI-MS: (M+H)+=363.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514974B2
Source datasetuspto-grants-2003_02
ORD IDord-e741b51d181448349de9ea61d20cabe3
Source noteuspto-grants-2003_02