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HRID 18283作成日:2026年10月25日

5-chloro-1-methyl-1H-indole-3-carbaldehyde → 5-chloro-1-methyl-3-(methylaminomethyl)-1H-indole

https://huagongshe.com/reaction/18283

反応式

関与物質

役割名称HCID仕込み量
反応物5-chloro-1-methyl-1H-indole-3-carbaldehydeHCID 16723796—
反応物Methyl 2-((5-bromopyridin-2-yl)amino)acetateHCID 22139049—
生成物5-chloro-1-methyl-3-(methylaminomethyl)-1H-indoleHCID 2213901793%

反応手順

According to the procedure of Preparation 13 (c), except substituting 5-chloro-1-methyl-1H-indole-3-carboxaldehyde for the ,3-dimethyl-1H-indole-2-carboxaldehyde, the title compound (2.1 g, 93%) was obtained as an amber oil: MS (ES) m/e 209.0 (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-1f60f64e365b4bac8c8133e5d94d27ce
出典メモuspto-grants-2010_06