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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170855Generated: October 31, 2026

Trifluoroacetic acid → (4-(Aminomethyl)pyridin-2-yl)(4-(4-chlorophenoxy)piperidin-1-yl)methanone

https://huagongshe.com/reaction/2170855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68204542HCID 68204542—
SolventDichloromethaneHCID 6344—
Product(4-(Aminomethyl)pyridin-2-yl)(4-(4-chlorophenoxy)piperidin-1-yl)methanoneHCID 67168014100%

Reaction Steps

A mixture of tert-butyl ((2-(4-(4-chlorophenoxy)piperidine-1-carbonyl)pyridin-4-yl)methyl)carbamate (165 mg, 0.37 mmol, Step-1), trifluoroacetic acid (2 mL), and dichloromethane (2 mL) was stirred at room temperature for 1 hour. After removal of the solvent, the residue was purified by a strong cation exchange cartridge (BondElute(registered trademark) SCX) to give 128 mg (>99%) of the title compound as colorless syrup. 25 mg of this material was further purified by preparative LC-MS to give 16.9 mg (68% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051296B2
Source datasetuspto-grants-2015_06
ORD IDord-bc77297318344b798fac17fb24a90332
Source noteuspto-grants-2015_06