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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196796Generated: November 1, 2026

Potassium Carbonate → HCID 178490673, compound

https://huagongshe.com/reaction/2196796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant[(2S)-5-oxopyrrolidin-2-yl]methyl 4-methylbenzene-1-sulfonateHCID 2734055—
Reactantn-(5-Tert-butylthiazol-2-yl)-5-chloro-2-methoxybenzamideHCID 87094486—
CatalystTetraethylammonium IodideHCID 6225—
CatalystTetrabutylammonium IodideHCID 67553—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventTolueneHCID 1140—
ProductHCID 178490673HCID 17849067348.5%

Reaction Steps

A mixture of Example 4C (810 mg, 2.49 mmol), (S)-(5-oxopyrrolidin-2-yl)methyl 4-methylbenzenesulfonate (Aldrich, 807 mg, 3 mmol), potassium carbonate (828 mg, 6 mmol), tetrabutylammonium iodide (20 mg, 0.05 mmol), tetrabutylammonium hydrogensulfate (20 mg, 0.06 mmol) and tetraethylammonium iodide (20 mg, 0.07 mmol) in anhydrous toluene (100 mL) was refluxed for 15 h. The mixture was cooled to room temperature, washed with water, brine, dried with anhydrous MgSO4, filtered, and concentrated under reduced pressure. The residue was chromatographed (SiO2, ethyl acetate-ethanol 9:1) to afford 510 mg of the title compound. 1H NMR (300 MHz, DMSO-d6) δ 1.32 (s, 9H), 1.83 (m, 1H), 2.07 (m, 3H), 3.78 (s, 3H), 4.09 (m, 2H), 4.30 (m, 1H), 7.10 (d, J=9 Hz, 1H), 7.27 (s, 1H), 7.45 (dd, J=9 Hz, 3 Hz, 1H), 7.62 (d, J=3 Hz, 1H), 7.82 (broad s, 1H); MS (DCI/NH3) m/z 422 (M+H)+. Anal. calcd for C20H24ClN3O3S.0.25H2O: C, 56.33; H, 5.79; N, 9.85. Found: C, 56.42; H, 5.55; N, 9.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338467B2
Source datasetuspto-grants-2012_12
ORD IDord-403f679a22464383b4441d3f041412a8
Source noteuspto-grants-2012_12