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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926472Generated: October 31, 2026

Toluene → 4-(3-(4-(1H-1,2,4-Triazol-1-yl)benzyl)-4-chloro-2-methoxyquinoline-6-carbonyl)benzonitrile

https://huagongshe.com/reaction/926472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium MethoxideHCID 10942334—
Reactant4-(3-(4-(1H-1,2,4-Triazol-1-yl)benzyl)-2,4-dichloroquinoline-6-carbonyl)benzonitrileHCID 118006116—
SolventDichloromethaneHCID 6344—
Product4-(3-(4-(1H-1,2,4-Triazol-1-yl)benzyl)-4-chloro-2-methoxyquinoline-6-carbonyl)benzonitrileHCID 118006247—

Reaction Conditions

Temperature110 °C

Reaction Steps

A heterogeneous mixture containing 4-(3-(4-(1H-1,2,4-triazol-1-yl)benzyl)-2,4-dichloroquinoline-6-carbonyl)benzonitrile (583 mg, 1.20 mmol, Intermediate 16: step d), sodium methoxide (780 mg, 14.4 mmol), and toluene (17 mL) was heated to 110° C. After 45 minutes, the flask was allowed to cool to 23° C. Dichloromethane (100 mL) was added to the flask and then the mixture was filtered through Celite®, rinsing with dichloromethane. Silica gel (5 g) was added to the filtrate and the solvent was removed by rotary evaporation to provide a free-flowing powder. The powder was loaded onto a column of silica gel for flash chromatography purification. Elution with hexanes initially, grading to 80% ethyl acetate-hexanes afforded the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284308B2
Source datasetuspto-grants-2016_03
ORD IDord-43c9cdc7298b47b2b3acd154e0b487ee
Source noteuspto-grants-2016_03