HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090657Generated: October 28, 2026
Water → 3-Butyryl-4-(2-methylphenylamino)-8-(3-dimethylaminopropoxy)quinoline
https://huagongshe.com/reaction/1090657
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 3-(Dimethylamino)propyl chloride hydrochloride | HCID 94308 | — |
| Reactant | 3-Butyryl-4-(2-methylphenylamino)8-hydroxyquinoline | HCID 10403732 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Butyryl-4-(2-methylphenylamino)-8-(3-dimethylaminopropoxy)quinoline | HCID 9931129 | 88% |
Reaction Steps
3-Butyryl-4-(2-methylphenylamino)-8-hydroxyquinoline (3.20 g, 10 mmol) and potassium t-butoxide (3.05 g, 25 mmol) were dissolved in dimethyl formamide (30 ml), warmed to 80° and 3-dimethylaminopropyl chloride hydrochloride (1.90 g, 12 mmol) added. The mixture was stirred for 1 hour at 80° then a further portion of potassium t-butoxide (2.44 g, 20 mmol) and 3-dimethylaminopropyl chloride hydrochloride (1.58 g, 10 mmol) added. After a further 2 hours at 80° the mixture was poured into water, extracted with ether and the ether extracts dried and evaporated. Chromatography (silica gel, 5% methanolic ammmonia in dichloromethane) and recrystallisation from ethyl acetate gave 3-butyryl-4-(2-methylphenylamino)-8-(3-dimethylaminopropoxy)quinoline (1.80 g, 88%), m.p. 109°-110°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05082841 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-a0d99f9223a44962bdc9254f3ae77b28 |
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| Source note | uspto-grants-1992_01 |
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