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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987175Generated: October 31, 2026

Diisopropylethylamine → HCID 44249374, compound

https://huagongshe.com/reaction/1987175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
Reactant1-(4-Amino-3-fluorophenyl)pyridin-2-oneHCID 22181548—
ReactantHCID 34180170HCID 34180170—
SolventAcetonitrileHCID 6342—
ProductHCID 44249374HCID 44249374—

Reaction Conditions

Temperature25 °C

Reaction Steps

Compound 7a (1.85 g; 6 mmol) is suspended in acetonitrile (20 ml) and N,N-diisopropyl ethyl amin (1.65 ml; 10 mmol) is added at 25° C. BOP-CL (2.46 g; 10 mmol) is added as a solid and after stirring for 30 min at 25° C. 1-(4-amino-3-fluoro-phenyl)-1H-pyridin-2-one (1.45 g; 7 mmol) is added to the reaction mixture. The mixture is stirred for 4 d at 25° C., evaporated to dryness and dissolved in ethyl acetate (200 ml). The organic phase is washed with 2 N HCl (50 ml), with 10% aqueous Na2CO3 solution, water and brine and dried over Na2SO4. The organic phase is filtered and the filtrate is evaporated to dryness. The crude product is purified by silica gel chromatography. Yield: 1.77 g (58.1%), ESI-MS: m/z=472 [M−H]−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550487B2
Source datasetuspto-grants-2009_06
ORD IDord-96509bd7381d43a3a521aa219c227dde
Source noteuspto-grants-2009_06