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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412405Generated: November 1, 2026

Ammonium Chloride → HCID 178438661, compound

https://huagongshe.com/reaction/1412405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178438660HCID 178438660—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178438661HCID 17843866174.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

4′-({5-Oxo-4-[trans-4-(2-oxobutoxy)cyclohexyl]-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (0.64 g) was dissolved in tetrahydrofuran (3 mL) and methanol (6 mL), and sodium tetrahydroborate (0.060 g) was added at 0° C. The reaction mixture was stirred at 0° C. for 2 hr. Saturated aqueous ammonium chloride solution was added to the reaction mixture, the solvent was evaporated under reduced pressure, and the residue was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.48 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-fd49a5498d024fce944b14daec77e4b2
Source noteuspto-grants-2014_12