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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005678Generated: November 1, 2026

Phosphorus oxychloride → HCID 22674092, compound

https://huagongshe.com/reaction/1005678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 22674130HCID 22674130—
SolventChloroformHCID 6212—
ProductHCID 22674092HCID 2267409249.4%

Reaction Steps

In chloroform (100 ml) was dissolved 3.0 g of 6-(4-toluenesulfonylamino)isoquinoline (Preparation Example 21), and m-chloroperbenzoic acid (2.57 g) was added thereto under ice-cooling, followed by stirring at room temperature overnight. The solvent was evaporated, and the resulting crystals were washed with diethyl ether, collected by filtration and dried, to give pale yellow crystals. The obtained crystals were suspended in chloroform (83 ml), and phosphorus oxychloride (19 ml) was added thereto, followed by heating under reflux for 5 hours. After cooling, the solvent was evaporated, and the residue was basified with an aquesou sodium bicarbonate in an ice-bath, followed by extracting with ethyl acetate, The extract was washed with brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The residue was purified by silica gel column, to give crude crystals of the title compound (1.630 g, 49.40%). The crude crysatals were recrystallized from ethanol, to give the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787534B2
Source datasetuspto-grants-2004_09
ORD IDord-7a63818d78584ea8903c0fe8b35f5602
Source noteuspto-grants-2004_09