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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494370Generated: October 31, 2026

4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonyl chloride → N-(4-benzoyl-1-ethyl-1H-pyrazol-3-yl)-4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonamide

https://huagongshe.com/reaction/494370

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonyl chlorideHCID 21090679—
Reactant(3-amino-1-ethyl-1H-pyrazol-4-yl)-phenyl-methanoneHCID 68866724—
SolventPyridineHCID 1049—
ProductN-(4-benzoyl-1-ethyl-1H-pyrazol-3-yl)-4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonamideHCID 11272705—

Reaction Steps

To a solution of the title A compound, (3-amino-1-ethyl-1H-pyrazol-4-yl)-phenyl-methanone (0.035 g, 0.16 mmol) in pyridine at RT, is added 4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonyl chloride (0.06 g, 0.16 mmol) in pyridine. The solution is stirred at RT for 16 h. The reaction mixture is concentrated, the residue is taken up into ethyl acetate, washed with 1 N HCl, water, saturated sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, filtered and concentrated at reduced pressure. The crude product is chromatographed on silica gel using 50% ethyl acetate in hexanes to yield N-(4-benzoyl-1-ethyl-1H-pyrazol-3-yl)-4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzenesulfonamide as a solid: MS [m/z] 541.1 [M-1]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538135B2
Source datasetuspto-grants-2009_05
ORD IDord-3db254b39d2c49c494b4b5df75605fc6
Source noteuspto-grants-2009_05