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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193451Generated: October 29, 2026

2,4-Difluorophenylboronic acid → HCID 53474283, compound

https://huagongshe.com/reaction/2193451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Difluorophenylboronic acidHCID 2734334—
ReactantHCID 59532381HCID 59532381—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 53474283HCID 5347428342%

Reaction Steps

To a solution of (S)-3-((R)-1-(4-bromophenyl)ethyl)-6-(4-fluorophenyl)-6-(2-hydroxyethyl)-1,3-oxazinan-2-one (109 mg, 0.26 mmol), 2,4-difluorophenylboronic acid (49 mg, 0.31 mmol) and Pd(PPh3)4 (30 mg, 0.03 mmol) in dioxane (8 mL) was added a solution of CsCO3 (2 M, 1 mL) at 0□. 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-((R)-1-(2′,4′-difluorobiphenyl-4-yl)ethyl)-6-(4-fluorophenyl)-6-(2-hydroxyethyl)-1,3-oxazinan-2-one (49 mg, 42%). LC-MS Method 3 tR=1.41, min, m/z=456; 1H NMR (CD3OD): 1.55 (m, 3H), 2.12 (m, 2H), 2.22-2.46 (m, 3H), 2.52 (m, 1H), 3.12 (m, 1H), 3.33 (m, 1H), 3.68 (m, 1H), 5.56 (m, 1H), 7.08 (m, 6H), 7.08 (m, 2H), 7.35 (m, 5H). 443-155-3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329897B2
Source datasetuspto-grants-2012_12
ORD IDord-15b9f9ea44374d1093cd047f5d3e86b5
Source noteuspto-grants-2012_12