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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428747Generated: November 2, 2026

Trifluoroacetic acid → HCID 86680218, compound

https://huagongshe.com/reaction/1428747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86680217HCID 86680217—
SolventDichloromethaneHCID 6344—
ProductHCID 86680218HCID 8668021883.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of tert-butyl 2-chloro-4-(1-oxo-1-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methylamino)propan-2-yl)benzylcarbamate (132 mg, 0.234 mmol) in dichloromethane (4 mL), cooled to 0° C., were added trifluoroacetic acid (2 ml). The resulting reaction mixture was stirred for 1 h at 0° C. and 1 hour at room temperature, then basified to pH 8-9 with aq. NaHCO3. The mixture was filtered using celite pad. The filtrate dissolved in dichloromethane and extracted with NaHCO3. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 2-(4-(aminomethyl)-3-chlorophenyl)-N-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (90 mg) was obtained as 83% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-28a18680687a427ba6cf2ebe43bd9364
Source noteuspto-grants-2015_01