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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592329Generated: October 31, 2026

Dimethylformamide → Methy 6-amino-4'-fluoro-5-[(2-hydroxy-2-methylpropyl)amino]biphenyl-3-carboxylate

https://huagongshe.com/reaction/592329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylamineHCID 7912—
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantMethy 4-amino-3-bromo-5-[(2-hydroxy-2-methylpropyl)amino]benzoateHCID 66693821—
Catalystpalladium(II) acetateHCID 167845—
Catalyst4,4',4''-Phosphinetriyltribenzenesulfonic acid sodiumHCID 131734552—
SolventWaterHCID 962—
ProductMethy 6-amino-4'-fluoro-5-[(2-hydroxy-2-methylpropyl)amino]biphenyl-3-carboxylateHCID 6669332770.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of methy 4-amino-3-bromo-5-[(2-hydroxy-2-methylpropyl)amino]benzoate (513 mg, 1.617 mmol), palladium(II) acetate (7.26 mg, 0.032 mmol), (4-fluorophenyl)boronic acid (453 mg, 3.23 mmol) and 4,4′,4″-phosphinetriyltribenzenesulfonic acid-sodium salt (48.8 mg, 0.097 mmol) were added DMF (2.43 mL) and water (0.809 mL) followed by diisopropylamine (0.461 mL, 3.23 mmol). The reaction was capped and heated at 80° C. for 2 h. The reaction was cooled, quenched with saturated sodium bicarbonate and diluted with EtOAc. The aqueous layers were washed with EtOAc (2×) and the combined organics were washed with water (3×) and brine (1×). Organics were dried over magnesium sulfate, filtered and concentrated. Purification by reverse phase HPLC (C-18, 95% water/acetonitrile→5% water/acetonitrile with 0.1% TFA) gave the title compound (377 mg): LC-MS [M+1]=333.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238647B2
Source datasetuspto-grants-2016_01
ORD IDord-e8f7bc8eed9a44e7a52b71be25df9a72
Source noteuspto-grants-2016_01