Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420680Generated: October 30, 2026

Sodium hydride → HCID 58001769, compound

https://huagongshe.com/reaction/420680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 58001797HCID 58001797—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 58001769HCID 5800176982.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl N-[2-[(2,2-dimethyl-1,3-dioxan-5-yl)amino]-6-(methyloxy)-3-pyridinyl]glycinate (35.42 g, 104.4 mmol) was dissolved in dry THF (500 ml) and the solution was added dropwise over 2 h to a cooled (0° C.) suspension of sodium hydride (4.173 g of 60% w:w dispersion in oil) in dry THF (500 ml) under argon. During the addition the colour of the suspension changed from orange to green. The mixture was stirred at 0° C. for a further 15 minutes, then allowed to warm to room temperature and stirred at rt for 1 h. The mixture was cooled to 0° C. and saturated NH4Cl (15 ml) was added cautiously with vigorous stirring (effervescence observed). After effervescence had ceased, the mixture was allowed to warm to room temperature and stirred for 4 h then diluted with EtOAc (500 ml) and filtered with suction. The solids were washed with EtOAc (300 ml) and the combined filtrate plus washings were evaporated under reduced pressure to give a dark brown solid. This was stirred with petroleum ether (40-60°) (500 ml) plus EtOAc (20 ml) and filtered with suction to give a lighter brown solid which was washed with petroleum ether (40-60°) (100 ml) and air-dried to afford the title compound (25.37 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097628B2
Source datasetuspto-grants-2012_01
ORD IDord-28e7f08f9ae94c288ce8f2824a8e4b52
Source noteuspto-grants-2012_01