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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876782Generated: November 1, 2026

Ammonia → 3-Amino-1-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-4-(2,4,5-trifluorophenyl)but-2-en-1-one

https://huagongshe.com/reaction/1876782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAmmonium AcetateHCID 517165—
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—
Product3-Amino-1-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-4-(2,4,5-trifluorophenyl)but-2-en-1-oneHCID 5340027375%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 7-(1,3-dioxo-4-(2,4,5-trifluorophenyl)-butyl)-3-trifluoromethyl-5,6,7,8-tetrahydro-1,2,4-triazolo[4,3-a]pyrazine (22.1 g), ammonium acetate (25 g), methanol (220 mL), and aqueous ammonia (22 mL) are heated to about 55° C. and stirred for about 6 hours. The reaction mass is then cooled to 30° C. and the undissloved particles are filtered off. The filterate is distilled off completely under vaccum. To the residue, ethanol (25 mL) is charged and the mixture is stirred at about 30° C. for about 30 minutes. The solid is filtered, washed with ethanol (5 mL), and dried to afford the title compound. (Yield: 75%; purity by HPLC: 96.7%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309724B2
Source datasetuspto-grants-2012_11
ORD IDord-133f3afd5ffe4e91bb01aeef811ba1d7
Source noteuspto-grants-2012_11