HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789413Generated: October 30, 2026
Isobutylamine → 4-Isobutylamino-3-nitroquinoline
https://huagongshe.com/reaction/1789413
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | 4-Chloro-3-nitroquinoline | HCID 11275808 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Isobutylamino-3-nitroquinoline | HCID 10999310 | — |
Reaction Steps
To a stirred solution of 50.Og (0.24 mole) of 4-chloro-3-nitroquinoline in 300 ml of tetrahydrofuran was added, in small portions, 52.7g (0.72 mole) of isobutylamine. The mixture was heated at its reflux temperature for one hour, and was then evaporated in vacuo. Water was added to the residue and the solid was separated by filtration. The solid was suspended in one liter of water, and was dissolved by the gradual addition of concentrated hydrochloric acid (to pH 3 to 4), at which time the solution was filtered. The filtrate was basified (to pH 9 to 10) by the addition of concentrated ammonium hydroxide to provide bright yellow 4-(isobutylamino)-3-nitroquinoline, m.p. 119°-121° C. The structural assignment was supported by infrared spectral analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04689338 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-2a25a670f29446a8bcfed9c8a1b1ea10 |
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| Source note | uspto-grants-1987_08 |
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