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HRID 1966537作成日:2026年10月27日

4-Chloro-8-methoxy-2-methylquinoline → (rac)-1-(4-Chlorophenyl)-N*1*-(8-methoxy-2-methylquinolin-4-yl)-N*2*,N*2*-dimethylethane-1,2-diamine dihydrochloride

https://huagongshe.com/reaction/1966537

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-8-methoxy-2-methylquinolineHCID 807583—
反応物(2-Amino-2-(4-chlorophenyl)ethyl)dimethylamineHCID 16643575—
溶媒Ethyl AcetateHCID 8857—
生成物(rac)-1-(4-Chlorophenyl)-N*1*-(8-methoxy-2-methylquinolin-4-yl)-N*2*,N*2*-dimethylethane-1,2-diamine dihydrochlorideHCID 13173051160.4%

反応手順

4-Chloro-8-methoxy-2-methylquinoline (2.00 g, 9.63 mmole), 1-(4-chlorophenyl)N*2*,N*2*-dimethylethane-1,2-diamine (2.30 g, 11.6 mmole), sodium tert-butylate (1.3 g, 13.5 mmole), tris(dibenzylidenaceton)-dipalladium(0) (0.18 g, 0.193 mmole) and 2-dicyclohexyl-phosphino-2(N,N-dimethylamino)biphenyl (0.27 g, 0.674 mmole) were stirred at 150° C. under nitrogen atmosphere in a microwave oven for 30 min. The reaction mixture was dissolved in ethyl acetate and filtered. The filtrate was extracted with water. The organic phases were dried, concentrated and the residue was purified using silica gel chromatography, eluting with dichloromethane:methanol 90:10. Precipitation in isopropanol/HCl and in ethyl acetate gave the product (1.55 g, 36%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08420670B2
出典データセットuspto-grants-2013_04
ORD IDord-12c7456afd1f4763b019a5b648c41308
出典メモuspto-grants-2013_04