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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748531Generated: October 30, 2026

Sodium hydride → HCID 178526264, compound

https://huagongshe.com/reaction/748531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 12050204HCID 12050204—
ReactantHCID 85873132HCID 85873132—
SolventDimethylformamideHCID 6228—
ProductHCID 178526264HCID 17852626482.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a suspension of sodium hydride (0.05 g, 1.2 mmol, 60% dispersion in oil, pre-washed with hexane) in N,N-dimethylformamide (3 mL) was added a solution of 5-pyridin-3-yl-1,3-dihydro-2H-indol-2-one (0.19 g, 0.90 mmol) in N,N-dimethylformamide (4 mL). The mixture was stirred for 20 min under nitrogen atmosphere. 2-Chloro-5-(morpholin-4-ylmethyl)pyridine 1-oxide (0.14 g, 0.60 mmol), dissolved in N,N-dimethylformamide (3 mL) was added dropwise and the mixture was stirred at room temperature for 2 h and then heated at 130° C. for 1.5 h. The solvent was evaporated in vacuo and the residue was partitioned between 2 M HCl and ethyl acetate and the phases were separated. The aqueous layer was alkalized by addition of NaHCO3 (s) and extracted with ethyl acetate. The organic layer was dried (Na2SO4) and the solvent was removed in vacuo affording 200 mg of the title compound as a yellow solid: MS (ES) m/z 403 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399780B2
Source datasetuspto-grants-2008_07
ORD IDord-bf24637a24874f8993ce87b74853f523
Source noteuspto-grants-2008_07