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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715936Generated: October 25, 2026

Water → tert-butyl 1-(4-(N-thiazol-2-ylsulfamoyl)phenyl)azetidin-3-ylcarbamate

https://huagongshe.com/reaction/1715936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-bromo-N-(1,3-thiazol-2-yl)benzene-1-sulfonamideHCID 669304—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantTert-butyl azetidin-3-ylcarbamate acetateHCID 21904480—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Producttert-butyl 1-(4-(N-thiazol-2-ylsulfamoyl)phenyl)azetidin-3-ylcarbamateHCID 5946646333.3%

Reaction Steps

Prepared according to general procedure 21. A solution of 4-bromo-N-(thiazol-2-yl)benzenesulfonamide (2.0 g, 6.3 mmol), tert-butyl azetidin-3-ylcarbamate acetate (1.61 g, 6.9 mmol) sodium tert-butoxide (2.55 g, 26.5 mmol), biphenyl-2-yl-di-tert-butylphosphine (224 mg, 0.76 mmol), and Pd2(dba)3 (172 mg, 0.19 mmol) in toluene (16 mL) was stirred at 75° C. for 16 h. The reaction mixture was poured into H2O, and the pH was adjusted to 6. The aqueous layer was extracted 4 times with CH2Cl2, and the organics were combined, washed with saturated aqueous NaCl solution, dried over MgSO4, and concentrated. Purification via silica gel chromatography using 50-70% EtOAc in hexanes gave tert-butyl 1-(4-(N-thiazol-2-ylsulfamoyl)phenyl)azetidin-3-ylcarbamate (0.86 g, 33%). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=411.0; tR=2.54 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799822B2
Source datasetuspto-grants-2010_09
ORD IDord-24e13ce0ebcf4ecd8c8b9186fb36e4f9
Source noteuspto-grants-2010_09