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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814446Generated: October 25, 2026

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

https://huagongshe.com/reaction/1814446

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 wahsed with water and brine, and then dried over magnesium sulfate. The solvent was evaporated, and the reuslting 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 numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-6288324fdc97402aae6eca58a325d1a1
Source noteuspto-grants-2005_04