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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75128Generated: October 29, 2026

Trifluoroacetic acid → 2-chloro-N-((R)-1-(2,4-dichlorophenyl)ethyl)-5-(1-((S)-3-piperidyl)-3,6-dihydro-2H-pyridin-4-yl)aniline

https://huagongshe.com/reaction/75128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86689043HCID 86689043—
SolventDichloromethaneHCID 6344—
Product2-chloro-N-((R)-1-(2,4-dichlorophenyl)ethyl)-5-(1-((S)-3-piperidyl)-3,6-dihydro-2H-pyridin-4-yl)anilineHCID 86689042—

Reaction Steps

Trifluoroacetic acid (1.5 mL) was added to a solution of (S)-t-butyl 3-(4-(4-chloro-3-((R)-1-(2,4-dichlorophenyl)ethylamino)phenyl)-5,6-dihydropyridin-1(2H)-yl)piperidine-1-carboxylate (0.83 g, 1.5 mmol) in dichloromethane (3 mL) at room temperature, and the solution was stirred for 1 h. Excess solvent was removed in vacuo, and the residue was diluted with dichloromethane. The organic layer was neutralized with aqueous saturated sodium bicarbonate solution, and the aqueous layer was further extracted with dichloromethane. The combined organic layers were dried (Na2SO4), filtered, and concentrated in vacuo. The crude product was used without further purification (0.65 g, 1.4 mmol, 96%). MS: (ES) m/z calculated for C24H29ClN3 [M+H]+ 464.1. found 464.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835419B2
Source datasetuspto-grants-2014_09
ORD IDord-fa61c1da88ca4e9ea279024b00166501
Source noteuspto-grants-2014_09