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HRID 430062作成日:2026年10月27日

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

https://huagongshe.com/reaction/430062

反応式

関与物質

役割名称HCID仕込み量
反応物PutrescineHCID 1045—
反応物2-Chloro-4-methoxyquinolineHCID 12369166—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Aminobut-1-ylamino)-4-methoxyquinolineHCID 1835370647%

反応手順

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+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06320051B1
出典データセットuspto-grants-2001_11
ORD IDord-918e11715e534a4cb6a78f499bb40b68
出典メモuspto-grants-2001_11