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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269563Generated: October 25, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant1-(3-Dimethylaminopropyl)ethylcarbodiimide hydrochlorideHCID 21982921—
Reactant2''-{[(4-Fluorophenyl)methyl]oxy}-5-[(methyloxy)carbonyl]-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-3-carboxylic acidHCID 58731014—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2''-{[(4-fluorophenyl)methyl]oxy}-5-{[(2-methylpropyl)amino]carbonyl}-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-3-carboxylateHCID 5873101551.8%

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446222B2
Source datasetuspto-grants-2008_11
ORD IDord-4047a240d5c644808cfa34e5e1c68e3f
Source noteuspto-grants-2008_11