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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384498Generated: October 31, 2026

Ammonium Chloride → HCID 178428856, compound

https://huagongshe.com/reaction/384498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant3-[(1,4-Dihydro-3-methyl-4-oxo-2-pyridinyl)methoxy]-5-[(tetrahydro-2H-pyran-4-yl)methoxy]benzonitrileHCID 68508382—
SolventDimethylformamideHCID 6228—
ProductHCID 178428856HCID 17842885658.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-[(3-methyl-4-oxo-1,4-dihydropyridin-2-yl)methoxy]-5-(tetrahydro-2H-pyran-4-ylmethoxy)benzonitrile (100 mg) in DMF (2 mL) were added sodium azide (18 mg) and ammonium chloride (15 mg), followed by stirring at 100° C. for 24 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in a 1M aqueous sodium hydroxide solution and washed with diethyl ether. The aqueous layer was adjusted to a pH of 2 by adding 1M hydrochloric acid, followed by extraction with chloroform and a mixed solvent of chloroform-methanol (5:1). The organic layer was washed with saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by thin layer chromatography (developer: chloroform/methanol=6/1) and washed with ethyl acetate to obtain 3-methyl-2-{[3-(tetrahydro-2H-pyran-4-ylmethoxy)-5-(1H-tetrazol-5-yl)phenoxy]methyl}quinolin-4(1H)-one (37 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367702B2
Source datasetuspto-grants-2013_02
ORD IDord-4cfb4f836b0c4993b823b6a1cfaa8241
Source noteuspto-grants-2013_02