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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450981Generated: October 31, 2026

2,4-Difluorophenylboronic acid → HCID 59532356, compound

https://huagongshe.com/reaction/450981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Difluorophenylboronic acidHCID 2734334—
ReactantHCID 59532383HCID 59532383—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59532356HCID 5953235626%

Reaction Steps

To a solution of (S)-3-((S)-1-(4-bromophenyl)propyl)-6-(4-fluorophenyl)-6-(2-hydroxy ethyl)-1,3-oxazinan-2-one (60 mg, 0.14 mmol), 2,4-difluorophenylboronic acid (26 mg, 0.17 mmol) and Pd(PPh3)4 (16 mg, 0.01 mmol) in dioxane (5 mL) was added a solution of CsCO3 (2 M, 1 mL) at 0° C. Then the reaction mixture was refluxed overnight under nitrogen. The reaction mixture was washed with water and then extract with CH2Cl2 twice. The combined organic phases were dried over Na2SO4, filtered and concentrated to give the residue, which was purified by preparative HPLC to afford (S)-3-((S)-1-(2′,4′-difluorobiphenyl-4-yl) propyl)-6-(4-fluorophenyl)-6-(2-hydroxyethyl)-1,3-oxazinan-2-one (17 mg, 26%). 1H NMR (CD3OD): 0.96 (m, 3H), 2.01 (m, 2H), 2.12 (m, 2H), 2.30 (m, 2H), 2.48 (m, 1H), 3.10 (m, 1H), 3.33 (m, 1H), 3.65 (m, 1H), 5.38 (m, 1H), 7.02 (m, 4H), 7.08 (m, 2H), 7.28 (m, 4H), 7.42 (m, 1H). 443-114-3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487094B2
Source datasetuspto-grants-2013_07
ORD IDord-50fb02a8a780471bb6b4d64413526cc4
Source noteuspto-grants-2013_07