HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704848Generated: October 30, 2026
Hydrochloric Acid → 4-Quinolinamine, 2-chloro-N-(2-methylpropyl)-3-nitro-
https://huagongshe.com/reaction/704848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloro-3-nitroquinoline | HCID 2785138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Quinolinamine, 2-chloro-N-(2-methylpropyl)-3-nitro- | HCID 10934813 | 90% |
Reaction Steps
A mixture of 2,4-dichloro-3-nitroquinoline (100 g) and N,N-dimethylformamide (180 mL) was stirred, and triethylamine (42 g, 4 eq) was added dropwise, followed by dropwise addition of 2-methylpropylamine (21.5 g, 0.7 eq). The mixture was stirred at room temperature until the reaction was completed as determined by gas chromatography. Aqueous hydrochloric acid (250 mL, 4N) was added with stirring. The resulting mixture was stirred and cooled to about 0° C. to precipitate the product. The precipitate was filtered, washed with water, and dried at reduced pressure to afford the product 2-chloro-N-(2-methylpropyl)-3-nitro-4-quinolinamine in about 90% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988815 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-919a4c5a9ee845f980bd4e7e70c3943e |
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| Source note | uspto-grants-1991_01 |
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