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HRID 1268875作成日:2026年10月26日

Dichloromethane → 1-(4-Amino-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanone

https://huagongshe.com/reaction/1268875

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Potassium CarbonateHCID 11430—
反応物4-MethoxybenzylamineHCID 75452—
反応物1-(4-Chloro-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanoneHCID 18446512—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
生成物1-(4-Amino-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanoneHCID 10265028—

反応条件

温度55 °C

反応手順

To a suspension of 1-(4-chloro-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanone 97 (61 mg, 0.21 mmol) and potassium carbonate (174 mg, 1.26 mmol) in DMF (1.8 mL) was added 4-methoxybenzylamine (85 μl, 0.64 mmol). The resultant mixture was heated at 50° C. for 6.75 h. After this time, 20 mL of a 1:1 mixture of dichloromethane and methanol was added and the resultant slurry was filtered. The filtrate was concentrated and the residue was dissolved in trifluoroacetic acid (7 mL). The resultant mixture was heated at 55° C. for 2.75 h. After this time, the reaction mixture was concentrated and the residue was purified by silica gel column chromatography (eluent: dichloromethane:MeOH:Et3N, 98.5:1.5:0.5) to give 98. 1H NMR (400 MHz, CDCl3) δ: 2.66 (s, 3H), 5.78–6.15 (br s, 2H), 7.37 (t, J=7.0 Hz, 1H), 7.45 (t, J=7.5 Hz, 2H), 7.54 (s, 1H), 8.0 (d, J=3.5 Hz, 2H), 8.56 (s, 1H). MS (EI) m/z (M+H+) 269.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07199119B2
出典データセットuspto-grants-2007_04
ORD IDord-4a0ccd46beb140648fb87e5163786105
出典メモuspto-grants-2007_04