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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251103Generated: October 25, 2026

Phosphorus oxychloride → 1-Chloro-3-(2,4,5-trimethoxyphenyl)isoquinoline

https://huagongshe.com/reaction/1251103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-methyl-2-toluamideHCID 75111—
Reactant2,4,5-TrimethoxybenzonitrileHCID 910015—
Product1-Chloro-3-(2,4,5-trimethoxyphenyl)isoquinolineHCID 22503489—

Reaction Steps

3-(2,4,5-Trimethoxyphenyl)isoquinolin-1-one obtained by reacting N-methyl-o-toluamide (1.50 g) and 2,4,5-trimethoxybenzonitrile (1.93 g) according to Example 10-1 was reacted with phosphorous oxychloride (10 ml) according to Example 10-2, to give 1-chloro-3-(2,4,5-trimethoxyphenyl)isoquinoline, which was then reacted with N-ethylpiperazine (15 ml) at 120° C. for 5 hr. The reaction solution was evaporated, and to the resulting residue were added ethyl acetate and water. The resulting organic layer was washed with water and brine, and then dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), to give the free compound of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-94a49c7bd06d422c95542a5d1ab6c55c
Source noteuspto-grants-2002_01