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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387939Generated: October 28, 2026

Diisopropylethylamine → 4-chloro-7-methoxy-N,N-dimethylquinoline-6-carboxamide

https://huagongshe.com/reaction/387939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantDimethylamine tetrahydrofuranHCID 22320367—
Reactant7-Methoxy-4-oxo-1,4-dihydroquinoline-6-carboxylic acidHCID 22936439—
Reactant7-Methoxy-4-chloro-quinoline-6-carbonyl chlorideHCID 22936575—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-7-methoxy-N,N-dimethylquinoline-6-carboxamideHCID 58931363—

Reaction Conditions

Temperature0 °C

Reaction Steps

After dissolving 7-methoxy-4-chloro-quinoline-6-carbonyl chloride synthesized by the method of Production Example 152-2 from 7-methoxy-4-oxo-1,4-dihydroquinoline-6-carboxylic acid (1.0 g) in tetrahydrofuran (60 ml), the solution was cooled to 0° C. Diisopropylethylamine (1.6 ml) and a 2.0 M dimethylamine tetrahydrofuran solution (3 ml) were added and the mixture was stirred overnight at room temperature. Water was added, extraction was performed 3 times with ethyl acetate, and the organic layers were combined, washed with water and saturated saline, dried over sodium sulfate and then dried under reduced pressure to obtain the title compound (933 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-20a45e5f3f5b4017b65ccd6a4a1d1d8b
Source noteuspto-grants-2013_02