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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062634Generated: November 1, 2026

Ammonium Chloride → HCID 178438651, compound

https://huagongshe.com/reaction/2062634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178438650HCID 178438650—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178438651HCID 17843865173.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

4′-({4-[trans-4-(2-Cyclopropyl-2-oxoethoxy)cyclohexyl]-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (0.23 g) was dissolved in tetrahydrofuran (2 mL) and methanol (4 mL), sodium tetrahydroborate (0.027 g) was added at 0° C., and the mixture was stirred at 0° C. for 1 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 (0.17 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283353B2
Source datasetuspto-grants-2012_10
ORD IDord-c59b8bf7e3a84848a66a21c1861ab618
Source noteuspto-grants-2012_10