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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341183Generated: October 31, 2026

4-Fluorophenylboronic acid → HCID 59320849, compound

https://huagongshe.com/reaction/341183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantN1-(5-Bromo-3-nitro-2-pyridinyl)-1,3-benzenediamineHCID 59320866—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
ProductHCID 59320849HCID 5932084962.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of PdCl2dppf (300 mg, 0.4 mmol), N-(5-bromo-3-nitro-pyridin-2-yl)-benzene-1,3-diamine (Preparation P1, 2.5 g, 8.2 mmol) and 4-fluorophenylboronic acid (1.4 g, 10 mmol) in DME (16 ml) and 2N Na2CO3 (16 ml) was deoxygenated by evacuate/fill N2 (×3), then stirred and heated at 80° C. under N2 for 4 hours. After cooling to RT the mixture was partitioned between EtOAc/H2O and then filtered through Celite. The organic layer was washed with brine (×1) then dried (MgSO4), filtered and evaporated. The residue was purified by chromatography on silica (10→50% EtOAc/petrol) to give the title compound (1.66 g) as a dark red/brown solid. 1H NMR (400 MHz, DMSO-d6): 9.85 (1H, s), 8.87 (1H, d), 8.70 (1H, d), 7.82 (2H, dd), 7.33 (2H, t), 7.02 (1H, t), 6.92-6.81 (2H, m), 6.40 (1H, d), 5.15 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895745B2
Source datasetuspto-grants-2014_11
ORD IDord-a6f5c4d9188b4c4a98bebddbfcc54b53
Source noteuspto-grants-2014_11