Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092964Generated: October 30, 2026

Trifluoroacetic acid → HCID 51049976, compound

https://huagongshe.com/reaction/2092964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPiperidineHCID 8082—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 58227488HCID 58227488—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 51049976HCID 5104997662%

Reaction Steps

N,N-Carbonyldiimidazole (790 mg, 4.87 mmol) (Fluka Chemie AG) was added to a solution of 2-phenylethynyl-thiazole-5-carboxylic acid (1.00 g, 4.36 mmol) [Intermediate 1] in tetrahydrofuran (17.4 mL) and stirred for 60 minutes. Piperidine (3.03 g, 35.6 mmol) and trifluoroacetic acid (295 μL, 3.83 mmol) were added and the mixture was stirred for 20 hours. The yellow solution was diluted with 150 mL of EtOAc and washed with 3.7 M HCl solution (5×30 mL), water (1×30 mL), 1.0 M K2CO3 (4×30 mL), water (2×30 mL), brine (1×30 mL), dried (Na2SO4) and concentrated to give a light tan solid (94% pure by LC/MS). The sample was further purified by silica gel chromatography over a 40 g SiO2 column using a gradient elution from 25% EtOAc in hexanes to 30% EtOAc in hexanes over 30 minutes to give title compound (2-phenylethynyl-thiazol-5-yl)-piperidin-1-yl-methanone (797 mg, 62%) as a light yellow powder. 1H NMR (300 MHz, CDCl3) δ 7.94 (s, 1H), 7.63-7.59 (m, 2H), 7.46-7.36 (m, 3H), 3.69-3.67 (m, 4H), 1.78-1.62 (m, 6H). LCMS (Method 1), RT=1.41. Calculated [M+H]+=297; Observed [M+H]+=297.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440837B2
Source datasetuspto-grants-2013_05
ORD IDord-c2040f73edcd470097fc602b7e4a13eb
Source noteuspto-grants-2013_05