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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 269563Erstellt: 25. Oktober 2026

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsobutylamineHCID 6558—
Edukt4-MethylmorpholineHCID 7972—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
Edukt1-(3-Dimethylaminopropyl)ethylcarbodiimide hydrochlorideHCID 21982921—
Edukt2''-{[(4-Fluorophenyl)methyl]oxy}-5-[(methyloxy)carbonyl]-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-3-carboxylic acidHCID 58731014—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 2''-{[(4-fluorophenyl)methyl]oxy}-5-{[(2-methylpropyl)amino]carbonyl}-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-3-carboxylateHCID 5873101551,8%

Reaktionsschritte

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

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07446222B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-4047a240d5c644808cfa34e5e1c68e3f
Quellennotizuspto-grants-2008_11