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HRID 272934作成日:2026年10月26日

Diisopropylethylamine → 1-{4-[3-(2,2-Dimethylpyrrolidin-1-yl)propoxy]phenyl}cyclohexanecarbonitrile

https://huagongshe.com/reaction/272934

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物2,2-DimethylpyrrolidineHCID 414773—
反応物HCID 23091704HCID 23091704—
反応物1-[4-(3-Bromo-propoxy)-phenyl]-cyclohexanecarbonitrileHCID 59837504—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物AmmoniaHCID 222—
生成物1-{4-[3-(2,2-Dimethylpyrrolidin-1-yl)propoxy]phenyl}cyclohexanecarbonitrileHCID 5983743117%

反応条件

温度180 °C

反応手順

A (1:3) mixture of 1-[4-(3-bromo-propoxy)-phenyl]-cyclohexanecarbonitrile and 1-[4-(3-chloro-propoxy)-phenyl]-cyclohexanecarbonitrile (150 mg, 0.54 mmol), N,N-diisopropylethylamine (188 μL, 1.08 mmol) and 2,2-dimethyl-pyrrolidine (131 mg, 1.08 mmol) in NMP (0.5 mL) was heated at 180° C. in the microwave (Smith Personal Synthesiser) for 600 seconds. The reaction mixture was quenched with water (15 mL) and extracted with ethyl acetate (2×15 mL), dried over Na2SO4, filtered and concentrated in vacuo. The compound was purified by column chromatography on Biotage® silica gel, eluting with dichloromethane:methanol:ammonia, 98:2:0.2 to 95:5:0.5 to give the title compound as a brown oil (31 mg, 17%). 1H NMR (400 MHz, CDCl3) δ7.38 (d, 2H), 6.90 (d, 2H), 4.04 (t, 2H), 2.78 (t, 2H), 2.54 (t, 2H), 2.16-2.12 (m, 2H), 1.94 (pentet, 2H), 1.90-1.64 (m, 11H), 1.20-1.34 (m, 1H), 0.98 (s, 6H); HRMS (ESI+) 341.2588 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456164B2
出典データセットuspto-grants-2008_11
ORD IDord-99f121676a1e4897ae779a4d906ebbbd
出典メモuspto-grants-2008_11