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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929308Generated: October 31, 2026

Sodium hydride → HCID 118023214, compound

https://huagongshe.com/reaction/929308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-OxazolidinoneHCID 73949—
ReactantHCID 89871667HCID 89871667—
SolventSodium ChlorideHCID 5234—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 118023214HCID 118023214—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of oxazolidin-2-one (0.038 g, 0.44 mmol) in DMF (3 mL) was added NaH (60% dispersion in oil, 0.011 g, 0.44 mmol). The mixture was stirred at a temperature of about 0° C. for 10 minutes, and 3-chloro-N-(3-chloro-1-(pyridin-3-yl)-1H- pyrazol-4-yl)-N-methyl propanamide (0.12 g, 0.40 mmol) was added. The resulting brown-yellow mixture was stirred at room temperature for two hours and diluted with saturated aqueous NH4Cl. The mixture was diluted with EtOAc and saturated aqueous NaCl solution. The organic phase was separated, and the aqueous phase extracted with EtOAc (2×50 mL). The combined EtOAc extracts was dried over MgSO4, filtered, and concentrated under reduced pressure to give light brown gum. The gum was purified on silica gel eluting with MeOH/CH2Cl2 to give the title compound F31 as a colorless oil (0.13 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09295260B2
Source datasetuspto-grants-2016_03
ORD IDord-5d7e538cb3a24f2da012ef446e874299
Source noteuspto-grants-2016_03