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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441692Generated: November 1, 2026

Trifluoroacetic acid → HCID 59164595, compound

https://huagongshe.com/reaction/1441692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 4-(2-oxoethyl)piperidine-1-carboxylateHCID 10353694—
Reactant2-Chloro-6-trifluoromethylbenzothiazoleHCID 11470419—
ReactantHCID 59164596HCID 59164596—
ReactantHCID 68406062HCID 68406062—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 59164595HCID 5916459535.8%

Reaction Steps

1.1 g 4-{2-[[2-(4-Cyano-3-methyl-phenyl)-ethyl]-(6-trifluoromethyl-benzothiazol-2-yl)-amino]-ethyl}-piperidine-1-carboxylic acid tert-butyl ester [prepared according to the method described in Example 1 and 5 from 4-(2-Amino-ethyl)-2-methyl-benzonitrile trifluoro acetate, N-boc-piperidinyl-4-acetaldehyde and 2-Chloro-6-trifluoromethyl-benzothiazole] were dissolved in 50 ml dichloromethane. 5 ml trifluoroacetic acid were added and the reaction mixture was stirred at room temperature for one hour. 150 ml ethyl acetate were added and the mixture was washed three times with saturated NaHCO3 solution. The organic layer was dried over MgSO4 and then the solvent was removed in vacuo. The residue was purified by RP-HPLC to obtain 325 mg 2-Methyl-4-{2-[(2-piperidin-4-yl-ethyl)-(6-trifluoromethyl-benzothiazol-2-yl)-amino]-ethyl}-benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655679B2
Source datasetuspto-grants-2010_02
ORD IDord-d22327a4dd2e4452884e5e6bcbc1c048
Source noteuspto-grants-2010_02