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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369353Generated: November 2, 2026

Ethanol → (8S)-2-{(E)-2-[6-methoxy-5-(4-methyl-1H-imidazol-1-yl)-pyridin-2-yl]vinyl}-8-(2-trifluoromethylphenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo-[1,5-a]pyridine mesylate

https://huagongshe.com/reaction/2369353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethanesulfonic AcidHCID 6395—
ReactantE-2212HCID 46854987—
Solventtert-Butyl methyl etherHCID 15413—
Product(8S)-2-{(E)-2-[6-methoxy-5-(4-methyl-1H-imidazol-1-yl)-pyridin-2-yl]vinyl}-8-(2-trifluoromethylphenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo-[1,5-a]pyridine mesylateHCID 46912967—

Reaction Steps

Mesylic acid (0.8 μL) was added to a mixed solution of (8S)-2-{(E)-2-[6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl]vinyl}-8-(2-trifluoromethylphenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridine (50 mg) in t-butyl methyl ether (0.8 mL)-ethanol (0.1 mL). The mixture was solidified as a result of stirring at room temperature for two hours. The solid was collected by filtration through a glass filter. The solid was washed with t-butyl methyl ether-ethanol (8:1) and then dried under reduced pressure at room temperature to obtain 51.9 mg of the title compound as pale yellow solid crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703954B2
Source datasetuspto-grants-2014_04
ORD IDord-7593e2911b9f46e4b1b17c05086ea97c
Source noteuspto-grants-2014_04