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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1098612생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1098612

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물FormaldehydeHCID 712—
반응물Potassium CarbonateHCID 11430—
반응물Sodium HydroxideHCID 14798—
반응물7-Fluoro-1H-indoleHCID 2774504—
용매Acetic AcidHCID 176—
생성물1-(7-Fluoro-1H-indol-3-yl)-N,N-dimethylmethanamineHCID 2490512974%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143300B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-554ffaa698dc49f989831814a088d201
출처 메모uspto-grants-2012_03