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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862646Generated: October 25, 2026

Water → Ethyl 6,7-dimethoxy-4-(3,4-dimethoxyphenyl)-2-(1,2,4-triazol-1-ylmethyl)quinoline-3-carboxylate 1-oxide

https://huagongshe.com/reaction/862646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-chloromethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylate 1-oxideHCID 21851158—
SolventDimethylformamideHCID 6228—
ProductEthyl 6,7-dimethoxy-4-(3,4-dimethoxyphenyl)-2-(1,2,4-triazol-1-ylmethyl)quinoline-3-carboxylate 1-oxideHCID 2209759950%

Reaction Steps

Oily sodium hydride (60%, 0.156 g) was added to a solution of 1H-1,2,4-triazole (0.27 g) in N,N-dimethylformamide (DMF)(20 ml), and the mixture was stirred at room temperature for 15 minutes. Then ethyl 2-chloromethyl-6,7-dimethoxy-4-(3,4-dimethoxyphenyl)quinoline-3-carboxylate 1-oxide (1.5 g) was added, and the mixture was stirred at 80° C. for 45 minutes. The reaction mixture was poured into water and extracted with dichloromethane. The dichloromethane layer was washed with water and dried over magnesium sulfate, and the solvent was evaporated. The residual oil was subjected to column chromatography on silica gel. The fractions eluted with chloroform/methanol (30/1, v/v) gave ethyl 6,7-dimethoxy-4-(3,4-dimethoxyphenyl)-2-(1,2,4-triazol-1-ylmethyl)quinoline-3-carboxylate 1-oxide (0.8 g, 50%) which was then recrystallized from dichloromethanehexane. Colorless prisms. mp. 221°-222° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719157
Source datasetuspto-grants-1998_02
ORD IDord-a2b86a6690ba4145bf61c639b3c7088f
Source noteuspto-grants-1998_02