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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545324Generated: October 29, 2026

Azetidine → HCID 24856141, compound

https://huagongshe.com/reaction/545324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzetidineHCID 10422—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 24855903HCID 24855903—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 24856141HCID 2485614179.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 79 mg (0.20 mmol) of N-(4-tert-butyl-thiazol-2-yl)-2-(6-chloro-pyridine-3-sulfonyl)-2-methyl-propionamide (example 265, Table 19) and 57.5 mg (0.42 mmol) of potassium carbonate in dioxane (2 mL) were added 27 μL (0.4 mmol) of azetidine. The reaction was heated in a sealed tube to 70° C. for 3 h. The solids were removed by filtration and rinsed with dioxane (5 mL). The filtrate was concentrated under reduced pressure and the residue purified by column chromatography (silica, eluent DCM, 5-10% ethyl acetate) to afford 67 mg of 2-(6-azetidin-1-yl-pyridine-3-sulfonyl)-N-(4-tert-butyl-thiazol-2-yl)-2-methyl-propionamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935715B2
Source datasetuspto-grants-2011_05
ORD IDord-945626f82d2f43d3b37afa1c07cc84b4
Source noteuspto-grants-2011_05