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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 269563생성일: 2026년 10월 26일

Isobutylamine → Methyl 2''-{[(4-fluorophenyl)methyl]oxy}-5-{[(2-methylpropyl)amino]carbonyl}-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-3-carboxylate

https://huagongshe.com/reaction/269563

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참여 물질

역할이름HCID투입량
반응물IsobutylamineHCID 6558—
반응물4-MethylmorpholineHCID 7972—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물1-(3-Dimethylaminopropyl)ethylcarbodiimide hydrochlorideHCID 21982921—
반응물2''-{[(4-Fluorophenyl)methyl]oxy}-5-[(methyloxy)carbonyl]-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-3-carboxylic acidHCID 58731014—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물Methyl 2''-{[(4-fluorophenyl)methyl]oxy}-5-{[(2-methylpropyl)amino]carbonyl}-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-3-carboxylateHCID 5873101551.8%

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A mixture of 2″-{[(4-fluorophenyl)methyl]oxy}-5-[(methyloxy)carbonyl]-5″-(trifluoromethyl)-1,1′:2′,1″-terphenyl-3-carboxylic acid (90 mg, 0.17 mmol), 4-methylmorpholine (34 mg, 45 μl, 0.34 mmol), 1-hydroxybenzotriazole hydrate (30 mg, 0.2 mmol), 1-(3-dimethylaminopropyl)-ethylcarbodiimide hydrochloride (38 mg, 0.2 mmol), and isobutylamine (25 mg, 34 ul, 0.34 mmol) in dichloromethane (3 ml) was stirred at room temperature for 2 hours. The mixture was diluted with ethyl acetate (10 ml), then washed with saturated NaHCO3, 2M HCl, water and brine. The organic phase was dried and evaporated. The residue was purified by chromatography in ethyl acetate/hexane (1:9-1:4) to give the title compound as a colourless solid (51 mg, 50%). LCMS: Rt=4.10 min. [M+H] 580

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07446222B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-4047a240d5c644808cfa34e5e1c68e3f
출처 메모uspto-grants-2008_11