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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10543Generated: October 25, 2026

Trifluoroacetic acid → 4-(1-Chloro-5-isoquinolyl)aminopiperidine trifluoroacetate

https://huagongshe.com/reaction/10543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(1-Chloro-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979829—
SolventDichloromethaneHCID 6344—
Product4-(1-Chloro-5-isoquinolyl)aminopiperidine trifluoroacetateHCID 21979875—

Reaction Steps

Deprotection was performed (room temperature, 2 hours) by using Intermediate 84 (81.9 mg) and a mixed solution of trifluoroacetic acid and methylene chloride (1:1, 2 ml). The solvent was evaporated under reduced pressure, and the residue was added with methanol (2 ml) and diethyl ether (6 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (64 mg) as yellow powdery crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-c7ab94fd6f5a4dc4b97d834fc0e5f2b3
Source noteuspto-grants-2006_08