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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446067Generated: November 1, 2026

Potassium Carbonate → HCID 68546653, compound

https://huagongshe.com/reaction/1446067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-5-((1H-1,2,3-Triazol-1-yl)methyl)-3-(3-fluoro-4-iodophenyl)oxazolidin-2-oneHCID 11257720—
ReactantHCID 68548991HCID 68548991—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 68546653HCID 6854665350%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-(3-Fluoro-4-iodo-phenyl)-5(R)-[1,2,3]triazol-1-ylmethyl-oxazolidin-2-one (90 mg, 0.232 mmol), 2-Nitro-6(S)-[5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridin-2-ylmethoxy]-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (108 mg, 0.278 mmol), K2CO3 (244 mg, 0.464 mmol) and Pd(PPh3)4 (27 mg, 0.023 mmol) were combined and suspended in DMF (2 ml) and water (0.2 ml). The mixture was heated to 60° C. for 1½ hours then quenched with sat. aqueous NH4Cl (2 mL) at rt. The mixture was diluted with EtOAc (10 mL) and washed with water (5 mL×5). The organic phases were dried (MgSO4) and concentrated. Column chromatography (2% MeOH/CH2Cl2) provided 60 mg (50%) of the title product as yellow solid. LCMS (ESI) m/z 523 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666864B2
Source datasetuspto-grants-2010_02
ORD IDord-829e50a7cb494ac99901704349a206ea
Source noteuspto-grants-2010_02