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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42304Generated: October 26, 2026

Dichloromethane → 2-Phenyl-5-(2-phenylpyrimidin-5-yl)oxazole

https://huagongshe.com/reaction/42304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriphenylphosphineHCID 11776—
Reactant2-Phenyl-1,3-oxazoleHCID 589280—
Reactant5-Bromo-2-phenylpyrimidineHCID 14387745—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
CatalystHCID 178418647HCID 178418647—
SolventWaterHCID 962—
Product2-Phenyl-5-(2-phenylpyrimidin-5-yl)oxazoleHCID 5925238511%

Reaction Conditions

Temperature60 °C

Reaction Steps

Silver carbonate (317 mg, 1.15 mmol), triphenylphosphine (16 mg, 0.06 mmol) and Pd(dppf)Cl2.CH2Cl2 (24 mg, 5 mole %) were stirred together at room temperature under nitrogen. 5-Bromo-2-phenylpyrimidine (163 mg, 0.69 mmol) was added followed by 2-phenyl-oxazole (84 mg, 0.58 mmol; prepared according to Ohnmacht, S. A. et al., Chemical Communications, 2008, 1241-1243). Finally water (6 mL) was added and the mixture heated for 18 hours at 60° C. The mixture was cooled to room temperature and filtered through Celite washing with DCM and acetone. Purification by silica gel flash chromatography (100% DCM) through a 12-g Silicycle® flash silica cartridge gave title compound as light yellow solid (19 mg, 11% yield); Rf 0.68 with DCM; melting point 228-231° C.; 1H-NMR (300 MHz; DMSO-d6) δ 9.39 (s, 2H), 8.45 (dd, 2H), 8.17 (dd, 2H), 8.11 (s, 1H), 7.54-7.65 (m, 6H); MS (ESI+) m/z 300 (M+1), (ESI−) m/z 298 (M−1); H-PGDS FPBA IC50: 125 μM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536185B2
Source datasetuspto-grants-2013_09
ORD IDord-dd6b0107a0a94b75b6b5a9128fef319d
Source noteuspto-grants-2013_09