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HRID 1062428생성일: 2026년 10월 27일

Triethylamine → Pentafluorophenyl 2-(2-chlorophenyl)-1-(4-chlorophenyl)-1h-imidazole-4-carboxylate

https://huagongshe.com/reaction/1062428

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물PentafluorophenolHCID 13041—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(2-chlorophenyl)-1-(4-chlorophenyl)-1H-imidazole-4-carboxylic acidHCID 21868804—
용매DichloromethaneHCID 6344—
생성물Pentafluorophenyl 2-(2-chlorophenyl)-1-(4-chlorophenyl)-1h-imidazole-4-carboxylateHCID 2228559933.5%

반응 단계

Step 1, 2-(2-Chlorophenyl)-1-(4-chlorophenyl)-1H-imidazole-4-carboxylic acid (1.5 g, 4.5 mmol) was dissolved in dichloromethane (40 mL). 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDCI, 946 mg, 4.95 mmol) and triethylamine (500 mg, 4.95 mmol) were added followed by pentafluorophenol (815 mg, 4.37 mmol). The mixture was stirred at rt under argon for one hour before it was washed with 5% HCl, sodium bicarbonate solution, and then brine. The organic layer was dried (MgSO4), filtered, and concentrated to give the crude product (1.26 g) which was chromatographed over silica gel (20% EtOAc in hexanes) to afford pentafluorophenyl 2-(2-chlorophenyl)-1-(4-chlorophenyl)-1H-imidazole-4-carboxylate (0.73 g, 32% yield): LC-MS m/z 499.0 (MH+), retention time 3.93 min (method 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06960601B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-886d796e2ebf4b25bc60492aad07d703
출처 메모uspto-grants-2005_11