Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497792Generated: October 30, 2026

Methyl benzenesulfonate → {3-[6-[2-(4-Cyano-phenyl)-2H-pyrazol-3-yl]-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino]-propyl}-trimethyl-ammonium benzenesulfonate

https://huagongshe.com/reaction/1497792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl benzenesulfonateHCID 6630—
Reactant4-{5-[2-(3-Dimethylamino-propylamino)-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-6-yl]-pyrazol-1-yl}-benzonitrileHCID 73051920—
SolventAcetoneHCID 180—
Product{3-[6-[2-(4-Cyano-phenyl)-2H-pyrazol-3-yl]-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino]-propyl}-trimethyl-ammonium benzenesulfonateHCID 7305208089.3%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of 4-{5-[2-(3-dimethylamino-propylamino)-7-methyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-6-yl]-pyrazol-1-yl}-benzonitrile (Ex. 28, 55 mg, 0.10 mmol) in acetone (0.44 mL) was added methylbenzenesulfonate (15 μL, 0.11 mmol) at ambient temperature. The reaction mixture was heated 55° C. for 1.5 hrs. The cooled reaction mixture was concentrated in vacuo to give a clear colorless oil. The oil thus obtained was triturated in diethyl ether and the resultant solid taken up in minimal EtOAc and Et2O added until a white solid formed. The precipitate was collected by filtration, washed with Et2O and dried in vacuo to yield the title compound as a white solid (64 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199984B2
Source datasetuspto-grants-2015_12
ORD IDord-ff8a2e09e4314ed18a7442eb7c809a05
Source noteuspto-grants-2015_12