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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007018Generated: October 28, 2026

Phosphorus oxychloride → HCID 22503597, compound

https://huagongshe.com/reaction/1007018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-methyl-2-toluamideHCID 75111—
Reactant1-EthylpiperazineHCID 79196—
Reactant2-MethoxyisonicotinonitrileHCID 7204887—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 22503597HCID 225035979.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 3-(2-methoxypyridin-4-yl)isoquinolin-1-one (1.22 g) obtained by reacting N-methyl-o-toluamide (2.90 g) and 4-cyano-2-methoxypyridine (2.60 g) according to the method of Example 10-1 was added phosphorus oxychloride (25.7 g), and the resulting mixture was heated at 100° C. for 2 hr. The reaction solution was evaporated, and to the resulting residue were added ethyl acetate and purified water The ethyl acetate layer was washed with water, an aqueous solution of saturated sodium bicarbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, and the resulting 1-chloro-3-(2-methoxyphenyl)isoquinoline was reacted as it was with N-ethylpiperazine (20 ml) at 120° C. for 8 hr. The reaction solution was evaporated, and to the resulting residue were added ethyl acetate and purified water. The ethyl acetate layer was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), to the free compound of the title compound as a pale yellow oil (0.62 g, yield; 9.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790844B2
Source datasetuspto-grants-2004_09
ORD IDord-e7131e040dbe4db48fe7b3713dda8abc
Source noteuspto-grants-2004_09