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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430062Erstellt: 26. Oktober 2026

Putrescine → 2-(4-Aminobut-1-ylamino)-4-methoxyquinoline

https://huagongshe.com/reaction/430062

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPutrescineHCID 1045—
Edukt2-Chloro-4-methoxyquinolineHCID 12369166—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(4-Aminobut-1-ylamino)-4-methoxyquinolineHCID 1835370647%

Reaktionsschritte

2-Chloro-4-methoxyquinoline (prepared as for 2-chloro-4-ethoxyquinoline but using methanol as solvent; 3.873 g, 20 mmol) and 1,4-diaminobutane (12.3 g, 140 mmol) were heated at 60° C. for 50 h. The solution was then reduced in volume in vacuo, and diluted with dichloromethane. The solid was filtered off and washed with dichloromethane. The filtrate was evaporated to dryness and purified by flash chromatography, eluting with 0-10% ‘10% ammonia in methanol’ in dichloromethane, to give 2-(4-aminobut-1-ylamino)-4-methoxyquinoline as a white solid (2.29 g, 47%). This material (2.142 g, 8.73 mmol) in concentrated hydrochloric acid (80 ml) was gently refluxed for 15 h, and then evaporated to dryness to give the title compound as a white foam (2.65 g, 99%); δH (CD3OD) 1.8-1.9 (4H, m), 2.95-3.05 (2H, m), 3.5-3.6 (2H, m), 6.36 (1H, s), 7.46 (1H, t), 7.7-7.9 (2H, m), 8.45(1H, d): MS (ES+) 232 (100%, MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06320051B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-918e11715e534a4cb6a78f499bb40b68
Quellennotizuspto-grants-2001_11