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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168866Generated: November 3, 2026

Trifluoroacetic acid → HCID 22560629, compound

https://huagongshe.com/reaction/1168866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86589088HCID 86589088—
SolventDichloromethaneHCID 6344—
ProductHCID 22560629HCID 22560629—

Reaction Steps

To a solution of the 4-({ethyl-[7-(2,2,2-trifluoro-acetylamino)-1,2,3,4-tetrahydro-naphthalen-2-yl]-amino}-methyl)-piperidine-1-carboxylic acid tert-butyl ester (800 mg, 1.7 mmol) in methylene chloride (20 mL) under an inert atmosphere was added trifluoroacetic acid (5 mL) and the solution was allowed to stir at room temperature for 1 h. The reaction was concentrated in vacuo and partitioned between 10% KOH and EtOAc. The organic layer was washed with brine, dried (MgSO4), and concentrated to afford N-[7-(ethyl-piperidin-4-ylmethyl-amino)-5,6,7,8-tetrahydro-naphthalen-2-yl]-2,2,2-trifluoro-acetamide as an oil which was used directly for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627644B2
Source datasetuspto-grants-2003_09
ORD IDord-fb72ad76f70d4077b08e28d6e0132e15
Source noteuspto-grants-2003_09