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HRID 339410作成日:2026年10月27日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 2,3,5,6-tetrafluoro-4-methyl-N-(2-methylcyclohexyl)benzamide

https://huagongshe.com/reaction/339410

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物2-MethylcyclohexylamineHCID 23432—
反応物p-Toluic acid, 2,3,5,6-tetrafluoro-HCID 69548—
反応物1-HydroxybenzotriazoleHCID 75771—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物2,3,5,6-tetrafluoro-4-methyl-N-(2-methylcyclohexyl)benzamideHCID 2512956590%

反応条件

温度0 °C

反応手順

2,3,5,6-tetrafluoro-p-toluic acid (4.00 g, 19.22 mmol), HOBt (5.19 g, 38.44 mmol) and EDCI (4.42 g 23.06 mmol) were mixed in 200 ml of anhydrous DCM and 30 ml of anhydrous DMF. The mixture was cooled to 0° C. and allowed to stir under Ar for 15 minutes. To the mixture was added 2-methylcyclohexanamine (3.05 mL, 23.06 mmol) and the reaction mixture was allowed to slowly warm to ambient temperature and stirred overnight. The reaction mixture was diluted with DCM, washed with 1N HCl, water, aqueous NaHCO3, water and brine, drying over MgSO4, filtration and removal of solvent in vacuo, afforded the crude product as a pale yellow solid Recrystallization (EtOH/H2O) and drying in vacuo gave 5.23 g of the title compound as a white solid (mixture of 2 diasteromers, 90%). 1H NMR (CDCl3) δ 0.95, 1.01 (d, J=7.0, 6.6 Hz, 3H) 1.1-2.1 (m, 9H), 2.29 (m, 3H), 3.70, 4.29 (m, 1H), 5.65, 5.92 (m, 1H). MS (304.1, M+H). m. p. 202-204° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895050B2
出典データセットuspto-grants-2014_11
ORD IDord-086c3649e49740e78a87023d7377d97e
出典メモuspto-grants-2014_11