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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386922Generated: October 26, 2026

Sodium Methoxide → Dimethyl-{3-[5-(4-trifluoromethyl-phenyl)-1H-[1,2,4]triazol-3-yl]-benzyl}-amine hydrochloride

https://huagongshe.com/reaction/1386922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantIsopropanol hydrochlorideHCID 21912024—
Reactant3-Dimethylaminomethyl-benzoic acid hydrazideHCID 63571374—
ReactantEthyl 4-(trifluoromethyl)benzene-1-carboximidate hydrochlorideHCID 68765138—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductDimethyl-{3-[5-(4-trifluoromethyl-phenyl)-1H-[1,2,4]triazol-3-yl]-benzyl}-amine hydrochlorideHCID 2171771910.5%

Reaction Steps

To an ethanolic suspension of 4-trifluoromethyl-benzimidic acid ethyl ester hydrochloride salt (761 mg, 3.0 mmol, 1.5 eq.) was added sodium methoxide (162 mg, 3 mmol) in ethanol (20 ml.) and the resulting mixture stirred for 30 min.at r.t. 3-dimethylaminomethyl-benzoic acid hydrazide (386 mg, 2.0 mmol) in ethanol was then added at 20° C., followed by heating to reflux for 16 hrs. Upon cooling, the product mixture was filtered, solvent was evaporated and the residue subjected to preparative reversed-phase HPLC purification using a YMC ODS-AQ column (20×50 mm) and a (0.1% trifluoroacetic acid) water-acetonitrile gradient (25 ml/min. flow rate). The pure fractions were concentrated and the product obtained was converted to the hydrochloride salt in ether by addition of excess 5N HCl/iPrOH solution (1 ml) followed by solvent evaporation and high vacuum drying to afford the title compound (79 mg, 0.21 mmol, 10% yield) as a white foam. MS: m/e=347.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265426B1
Source datasetuspto-grants-2001_07
ORD IDord-180669cf5f534f7d858f979f1b187d11
Source noteuspto-grants-2001_07