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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1267123생성일: 2026년 10월 27일

4'-(Trifluoromethyl)(1,1'-biphenyl)-2-carboxylic acid → 4'-Trifluoromehtyl-biphenyl-2-carboxylic acid [4-[4-(3-cyano-benzyl)-piperazin-1-yl]-phenyl]-amide

https://huagongshe.com/reaction/1267123

반응식

참여 물질

역할이름HCID투입량
반응물4'-(Trifluoromethyl)(1,1'-biphenyl)-2-carboxylic acidHCID 55251—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-[4-(3-Cyano-benzyl)-piperazin-1-yl]-phenylamineHCID 11185447—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물4'-Trifluoromehtyl-biphenyl-2-carboxylic acid [4-[4-(3-cyano-benzyl)-piperazin-1-yl]-phenyl]-amideHCID 980731590.9%

반응 단계

To a stirred solution of 4-[4-(3-cyano-benzyl)-piperazin-1-yl]-phenylamine (0.29 g), 4′-trifluoromethyl-biphenyl-2-carboxylic acid (0.26 g), HOBt (0.16 g), and Et3N (0.12 g) in CH2Cl2 (15 mL) was added at room temperature EDCl (0.23 g) and the mixture was stirred at room temperature for 4 hours. The organic solution was then washed with water, with a saturated solution of NaHCO3 and dried over Na2SO4. After filtration and evaporation of the filtrate, the residue was purified by flash chromatography eluting with CH2Cl2/AcOEt (90/10) and the solid obtained was recrystallized from EtOH to give the title compound (0.48 g) as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06552022B1
출처 데이터셋uspto-grants-2003_04
ORD IDord-7e2b3068d1ed4ab4bbaf7da4cd15c816
출처 메모uspto-grants-2003_04