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HRID 77442作成日:2026年10月25日

Benzenemethanamine, 3,4-dichloro- → Methyl 6-(3,4-dichlorobenzylamino)nicotinate

https://huagongshe.com/reaction/77442

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenemethanamine, 3,4-dichloro-HCID 1608—
反応物Methyl 6-chloropyridine-3-carboxylateHCID 254249—
溶媒EthanolHCID 702—
生成物Methyl 6-(3,4-dichlorobenzylamino)nicotinateHCID 8667972733%

反応条件

温度120 °C

反応手順

A mixture of (3,4-dichlorophenyl)methanamine (1.010 mL, 7.58 mmol), TEA (1.218 mL, 8.74 mmol), and methyl 6-chloronicotinate (1 g, 5.83 mmol) in ethanol (29 mL) was heated at 120° C. for 5 min in a microwave oven. The reaction mixture was further heated at 100° C. for 54 h, then concentrated. The residue was purified by flash chromatography on silica gel using 5-35% ethyl acetate in hexanes. The desired fractions were concentrated to give methyl 6-(3,4-dichlorobenzylamino)nicotinate as a pale yellow solid (0.55 g, 33%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.77 (1H, s), 8.01 (1H, dd, J=8.78, 2.01 Hz), 7.33-7.52 (2H, m), 7.19 (1H, d, J=8.03 Hz), 6.37 (1H, d, J=8.78 Hz), 5.37 (1H, br. s.), 4.58 (2H, d, J=6.02 Hz), 3.88 (3H, s). LCMS: R.T.=2.81; [M+H]+=311.18.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841301B2
出典データセットuspto-grants-2014_09
ORD IDord-315f4008d95f4cddbbd565fc70894b6d
出典メモuspto-grants-2014_09