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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062748Generated: November 2, 2026

2-Dimethylaminopyridine → HCID 22281888, compound

https://huagongshe.com/reaction/1062748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
Reactant4-t-Butylbenzenesulfonyl chlorideHCID 139882—
Reactant5-amino-4-(1,3-benzodioxol-5-yl)-3-methoxy-1-methyl-1H-pyrazol-3-olHCID 22281908—
SolventPyridineHCID 1049—
ProductHCID 22281888HCID 222818886%

Reaction Steps

4-(tert-butyl)benzenesulfonyl chloride (190 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-pyrazol-3-ol (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 (10 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962923B2
Source datasetuspto-grants-2005_11
ORD IDord-5537ed06b4e14c07b76497f56791e1dc
Source noteuspto-grants-2005_11