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HRID 31515作成日:2026年10月27日

Dimethylformamide → 2-{4-[4,5-bis-(4-chloro-phenyl)-2-(2-ethoxy-4-trifluoromethyl-phenyl)-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-N-methyl-acetamide

https://huagongshe.com/reaction/31515

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物2-chloro-N,N-dimethylacetamideHCID 75886—
反応物DiisopropylethylamineHCID 81531—
反応物4,5-bis-(4-chloro-phenyl)-2-(2-ethoxy-4-trifluoromethyl-phenyl)-4,5-dihydro-1H-imidazoleHCID 10174168—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-{4-[4,5-bis-(4-chloro-phenyl)-2-(2-ethoxy-4-trifluoromethyl-phenyl)-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-N-methyl-acetamideHCID 11215985—

反応条件

温度65 °C

反応手順

2-Chloro-N,N-dimethyl-acetamide (0.0194 mmol) in dimethylformamide (0.25 mL) was pipeted into a 4 mL vial containing a solution of 4,5-bis-(4-chloro-phenyl)-2-(2-ethoxy-4-trifluoromethyl-phenyl)-4,5-dihydro-1H-imidazole (0.0169 mmol, example 1) and diisopropylethylamine (0.0194 mmol) in 0.25 mL of dimethylformamide. The vial was capped and heated to 65° C. for 2 d. The reaction was diluted with 1.5 mL of methylene chloride and 0.5 mL of water. The vial was agitated and centrifuged. The organic layer was transferred to a 4 mL vial and concentrated in vacuo to give 2-{4-[4,5-bis-(4-chloro-phenyl)-2-(2-ethoxy-4-trifluoromethyl-phenyl)-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-N-methyl-acetamide. LR-MS: 663 [(M+H)+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425638B2
出典データセットuspto-grants-2008_09
ORD IDord-6f86b4070d744a36ba17e54f5766a229
出典メモuspto-grants-2008_09