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HRID 443066作成日:2026年10月26日

Triethylamine → [3,5-Bis(trifluoromethyl)phenyl][3-(3,4-dichlorophenyl)piperazin-1-yl]methanone

https://huagongshe.com/reaction/443066

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3,5-Bis(trifluoromethyl)benzoic acidHCID 12889—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物2-(3,4-Dichlorophenyl)piperazineHCID 4231356—
溶媒DichloromethaneHCID 6344—
生成物[3,5-Bis(trifluoromethyl)phenyl][3-(3,4-dichlorophenyl)piperazin-1-yl]methanoneHCID 1961020853%

反応手順

To a cooled solution of CH2Cl2 (103 mL) containing 2-(3,4-dichlorophenyl)piperazine (1.15 g 5.0 mmol), 3,5-bis-(trifluoromethyl)benzoic acid (1.34 g, 5.09 mmol), and N-hydroxybenzotriazole monohydrate (0.688 g, 5.09 mmol) at -20° C. were added Et3N (0.711 mL 5.09 mmol) and N,N-dimethylaminopropyl-ethylcarbodimide (DEC) (0.967 g, 5.09 mmol) under nitrogen. The reaction was kept at -20° C. for an hour and gradually warmed to RT overnight. After stirring 20 h, the reaction was complete and CH2Cl2 (200 mL) was added. The organic solution was washed with 5% NaHCO3 (80 mL) and brine (80 mL, 2×), dried over MgSO4, filtered and concentrated under vacuum to give 2.1 g of crude product. The product was purified by flash chromatography on flash grade silica gel (120 g), eluting with 2% NH3 -MeOH/CH2Cl2 to give a foam solid (1.25 g, 2.65 mmol, 53%). m.p. 50°-53° C.; FAB MS [M+1]+ 470.9;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05892039
出典データセットuspto-grants-1999_04
ORD IDord-270b00f8d32a4ffc8d7cede32de8f96b
出典メモuspto-grants-1999_04