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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Dimethylamine tetrahydrofuran | HCID 22320367 | — |
| Reactant | 7-Methoxy-4-oxo-1,4-dihydroquinoline-6-carboxylic acid | HCID 22936439 | — |
| Reactant | 7-Methoxy-4-chloro-quinoline-6-carbonyl chloride | HCID 22936575 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-chloro-7-methoxy-N,N-dimethylquinoline-6-carboxamide | HCID 58931363 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372981B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-20a45e5f3f5b4017b65ccd6a4a1d1d8b |
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| Source note | uspto-grants-2013_02 |
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