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HRID 401601作成日:2026年10月23日

Dimethylamine → 1-(7-Fluoro-1H-indol-3-yl)-N,N-dimethylmethanamine

https://huagongshe.com/ja/reaction/401601

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物FormaldehydeHCID 712—
反応物Potassium CarbonateHCID 11430—
反応物Sodium HydroxideHCID 14798—
反応物7-Fluoro-1H-indoleHCID 2774504—
溶媒Acetic AcidHCID 176—
生成物1-(7-Fluoro-1H-indol-3-yl)-N,N-dimethylmethanamineHCID 2490512974%

反応手順

To a mixture of acetic acid (13.6 mL) and formaldehyde (0.340 mL, 4.5 mmol, 37% solution) under argon was added dimethyl amine (2.05 mL, 16.3 mmol., 40% solution). The reaction mixture was stirred for 10 min and then treated with 7-fluoroindole (540 mg, 4.0 mmol.). The resulting mixture was stirred at room temperature for ˜16 h. The reaction mixture was first neutralized with K2CO3 and then basified with NaOH (2N), and then extracted in ethyl acetate, washed with water, dried, and concentrated. Solid obtained was recrystallized from ethyl acetate and hexane to give (7-Fluoro-1H-indol-3-ylmethyl)dimethylamine (570 mg, 74%): mp 133-137° C., 1H NMR (500 MHz, CDCl3): 2.31 (s, 6H), 3.62 (s, 2H), 6.88-6.92 (dd, J=8.0 and 8.0 Hz, 1H), 7.00-7.04 (m, 1H), 7.16 (d, J=2.5 Hz, 1H), 7.46 (d, J=8.0 Hz, 1H), 8.34 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741942B2
出典データセットuspto-grants-2014_06
ORD IDord-6711a7e76634456d918f9239b1ac69bc
出典メモuspto-grants-2014_06