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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445983Generated: October 26, 2026

Ammonium Chloride → HCID 45110549, compound

https://huagongshe.com/reaction/445983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantSodiumHCID 5360545—
Reactant1-(3-(trifluoromethyl)-5,6-dihydro(1,2,4)triazolo(4,3-a)pyrazin-7(8H)-yl)-4-(2,4,5-trifluorophenyl)butane-1,3-dioneHCID 9887588—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 45110549HCID 45110549—

Reaction Conditions

Temperature-4 °C

Reaction Steps

In a 500 mL round bottom flask THF (50 mL) and methanol (100 mL) were taken. To the solution sodium salt of 4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-one (2.0 g) was added. It was cooled to −78 to 70° C. in a dry-ice bath. Then NaBH4 (0.7 g) was added in small lots in 10-15 min. It was stirred at −78 to 70° C. for 3-4 h. Reaction mixture was poured into aq. saturated NH4Cl solution at 0-5° C. Product was extracted with ethyl acetate. Organic layer was collected and dried over anhydrous sodium sulfate. Solvent was evaporated at reduced pressure to obtain the product. (Wt.-2.0 g, % Y-100%, % Purity by HPLC-95.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476437B2
Source datasetuspto-grants-2013_07
ORD IDord-71e24d0cb89d40ce949d2620adc4e7f4
Source noteuspto-grants-2013_07