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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353875Generated: November 1, 2026

Phenylboronic Acid → Isopropyl 5-[acetyl-(3,5-bistrifluoromethylbenzyl)amino]-8-phenyl-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate

https://huagongshe.com/reaction/2353875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantPotassium FluorideHCID 522689—
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
ReactantIsopropyl 5-[acetyl-(3,5-bistrifluoromethylbenzyl)amino]-8-bromo-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylateHCID 59003154—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductIsopropyl 5-[acetyl-(3,5-bistrifluoromethylbenzyl)amino]-8-phenyl-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylateHCID 5900314873%

Reaction Steps

Add a solution of isopropyl-5-[acetyl-(3,5-bistrifluoromethylbenzyl)amino]-8-bromo-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate (0.080 g, 0.134 mmol) in tetrahydrofuran (1 mL) to phenylboronic acid (0.024 g, 0.202 mmol), palladium acetate (0.0015 g, 0.0067 mmol), 2-(dicyclohexylphosphino)biphenyl (0.0047 g, 0.013 mmol) and potassium fluoride (0.023 g, 0.403 mmol) and purge with nitrogen and stir for 2 h at room temperature, then at 50° C. for 12 h. After this initial period, additional phenylboronic acid (0.024 g, 0.202 mol), palladium acetate (0.0015 g, 0.0067 mmol), 2-(dicyclohexylphosphino)biphenyl (0.0047 g, 0.013 mmol) and potassium fluoride (0.023 g, 0.403 mmol) is added and the reaction is heated at 50° C. for 1 h. Cool the reaction to room temperature and dilute with ethyl acetate (30 mL) and wash with 2 N sodium hydroxide and brine (10 mL each). Dry the organic layer over sodium sulfate, filter and remove the solvent under reduced pressure. Purify the residue using chromatography on silica gel, eluting with hexanes/ethyl acetate (60:40), to provide the title compound as a white solid (0.058 g, 72%): ESI MS 593 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749992B2
Source datasetuspto-grants-2010_07
ORD IDord-cb66cc1488e547a98bf98d7a3ba0edaa
Source noteuspto-grants-2010_07