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HRID 18271作成日:2026年10月24日

ethyl 4,6-dichloro-1-methyl-1H-indole-2-carboxylate → N,1-dimethylindole-2-carboxamide

https://huagongshe.com/ja/reaction/18271

反応式

関与物質

役割名称HCID仕込み量
反応物ethyl 4,6-dichloro-1-methyl-1H-indole-2-carboxylateHCID 22139053—
反応物Monomethylamine methanolHCID 57454252—
生成物N,1-dimethylindole-2-carboxamideHCID 1230331599%

反応条件

温度50 °C

反応手順

A suspension of ethyl 4,6-dichloro-1-methyl-1H-indole-2-carboxylate (1.06 g, 3.90 mmole) in 2.0 M CH3NH2/CH3OH (40 mL) in a sealed pressure bottle was heated in an oil bath preset at 50° C. A homogeneous solution formed within 2.5 hr. The reaction was kept at 50° C. for 17.5 hr, during which time a solid precipitated. The mixture was cooled to RT and poured into H2O (40 mL). The resulting mixture was concentrated on the rotavap to remove the methanol, and the solid was collected by suction filtration. This was washed with plenty of H2O and dried in high vacuum at 45-50° C. to afford the title compound (0.99 g, 99%) as an off-white solid: 1H NMR (400 MHz, CDCl3) δ 7.29 (s, 1 H), 7.16 (d, J=1.5 Hz, 1 H), 6.86 (s, 1 H), 6.21 (br s, 1 H), 4.02 (s, 3 H), 3.02 (d, J=4.9 Hz, 3 H); MS (ES) m/e 257 and 259 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741339B2
出典データセットuspto-grants-2010_06
ORD IDord-aa345c6a0d774baf803d5bbb2876f9e1
出典メモuspto-grants-2010_06