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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368603Generated: November 3, 2026

2-Dimethylaminopyridine → HCID 22281888, compound

https://huagongshe.com/reaction/1368603

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 numberUS06573270B1
Source datasetuspto-grants-2003_06
ORD IDord-c478f6acfafd4114a7fc151432174909
Source noteuspto-grants-2003_06