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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062750Generated: October 27, 2026

2-Dimethylaminopyridine → N-[4-(1,3-benzodioxol-5-yl)-3-methoxy-1-methyl-1H-pyrazol-5-yl]-4-isopropylbenzenesulfonamide

https://huagongshe.com/reaction/1062750

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
Reactant4-(Propan-2-yl)benzene-1-sulfonyl chlorideHCID 2734882—
Reactant5-amino-4-(1,3-benzodioxol-5-yl)-3-methoxy-1-methyl-1H-pyrazoleHCID 22281943—
SolventPyridineHCID 1049—
ProductN-[4-(1,3-benzodioxol-5-yl)-3-methoxy-1-methyl-1H-pyrazol-5-yl]-4-isopropylbenzenesulfonamideHCID 222819736.9%

Reaction Steps

4-Isopropylbenzenesulfonyl chloride (176 mg) was added at room temperature under an atmosphere of nitrogen to a solution of 5-amino-4-(1,3-benzodioxol-5-yl)-3-methoxy-1-methyl-1H-pyrazole (Preparation 43) (100 mg) and dimethylaminopyridine (50 mg) in anhydrous pyridine (4 ml). The reaction was stirred overnight. The mixture was concentrated under reduced pressure, then a saturated solution of ammonium chloride (6 ml), ethyl acetate (6 ml), and brine (6 ml) were sequentially added. The aqueous phase was extracted with ethyl acetate (2*8 ml) and the combined organic fractions were washed with brine (10 ml), dried over sodium sulfate and concentrated under reduced pressure. The residue was purified to yield the title compound (11.9 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962923B2
Source datasetuspto-grants-2005_11
ORD IDord-6f65e98fbc844421ac2a523db7b98e86
Source noteuspto-grants-2005_11