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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517976Generated: October 31, 2026

2-chloro-N,N-dimethylacetamide → HCID 70945201, compound

https://huagongshe.com/reaction/517976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-chloro-N,N-dimethylacetamideHCID 75886—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-methyl-6-(6-(2-(piperidin-4-yl)ethoxy)-5-(trifluoromethyl)pyridin-3-yl)-1H-[1,2,3]triazolo[4,5-c]pyridine-4-carbonitrile trifluoroacetateHCID 86673351—
SolventAcetonitrileHCID 6342—
ProductHCID 70945201HCID 7094520188.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 1-methyl-6-(6-(2-(piperidin-4-yl)ethoxy)-5-(trifluoromethyl)-pyridin-3-yl)-1H-[1,2,3]triazolo[4,5-c]pyridine-4-carbonitrile trifluoroacetate (200 mg) and N,N-diisopropylethylamine (310 μl) in acetonitrile (8 ml), 2-chloro-N,N-dimethylacetamide (77 μl, 91 mg) was added and the mixture stirred at 20° C. for 65 h. The reaction mixture was concentrated. The residue diluted with water (20 ml) and extrated with DCM (50 ml×3), combined DCM layer dried over sodium sulphate and solvent removed under reduced pressure. The residue was then purified by Strata Si column (5 g, dichloromethane:methanol=1:0, 25:1 to 15:1), converted to hydrochloric acid salt using 2N hydrochloric acid in diethyl ether to give 1-methyl-6-(6-(2-(1-(2-dimethylamino-2-oxo-ethyl)piperidin-4-yl)ethoxy)-5-(trifluoromethyl)pyridin-3-yl)-1H-[1,2,3]triazolo[4,5-c]pyridine-4-carbonitrile hydrochloride (179 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115126B2
Source datasetuspto-grants-2015_08
ORD IDord-e04a2a945f564b1db4571999ca5d01d3
Source noteuspto-grants-2015_08