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HRID 1630976作成日:2026年10月26日

2-Methylpiperidine → 4-(2-Methylpiperidin-1-YL)-3-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/1630976

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethylpiperidineHCID 7974—
反応物4-Fluoro-3-(trifluoromethyl)benzonitrileHCID 144255—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Diethyl EtherHCID 3283—
生成物4-(2-Methylpiperidin-1-YL)-3-(trifluoromethyl)benzonitrileHCID 58554130—

反応条件

温度100 °C

反応手順

A mixture of 4-fluoro-3-(trifluoromethyl)benzonitrile (50.0 g, 0.26 mol, Combi-Blocks AN-1049) and 2-methylpiperidine (156 mL, 1.32 mol) in DMSO (500 mL) was heated at 100° C. under nitrogen for 12 hours. The reaction mixture was diluted with Et2O and washed with water, a saturated aqueous solution of NaHCO3 and a saturated aqueous solution of NH4Cl. The organic layer was dried (MgSO4) and the solvent was removed under reduced pressure to give the title compound as a beige powder. UPLC/MS, M−(ESI): 269.2. 1H NMR (DMSO-d6, 300 MHz) δ 8.19 (d, J=2.0 Hz, 1H), 8.12 (dd, J=8.4, 2.0 Hz, 1H), 7.75 (d, J=8.2 Hz, 1H), 3.13 (m, 1H), 2.88 (m, 1H), 2.56 (m, 1H), 1.77-1.25 (m, 6H), 0.72 (d, J=6.0 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08791142B2
出典データセットuspto-grants-2014_07
ORD IDord-bc9f0ffe739b450aafd49f1d62c39d4d
出典メモuspto-grants-2014_07