Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48978Generated: October 26, 2026

Pyridine → 3-(3,5-Dimethylpyrazol-1-yl)-5-nitro-1,2-benzisothiazole

https://huagongshe.com/reaction/48978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3,5-DimethylpyrazoleHCID 6210—
Reactant1,2-Benzisothiazole, 3-chloro-5-nitro-HCID 198098—
SolventEthyl AcetateHCID 8857—
Product3-(3,5-Dimethylpyrazol-1-yl)-5-nitro-1,2-benzisothiazoleHCID 2063426643.8%

Reaction Steps

A mixture of 3-chloro-5-nitrobenzisothiazole (5.3 g, mmol), 3,5-dimethylpyrazole (2.40 g, 25.0 mmol) and pyridine is stirred overnight at reflux, cooled to room temperature and diluted with ethyl acetate. The resultant mixture is filtered and the filtrate is washed with three portions of 10% hydrochloric acid and one portion of water. The organic layer is dried over anhydrous magnesium sulfate and concentrated in vacuo to afford the title compound (2.85 g, 43.8%) which is identified by NMR spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706663B2
Source datasetuspto-grants-2004_03
ORD IDord-2faec26a94d54e92a133e6d5e439322b
Source noteuspto-grants-2004_03