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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484437Generated: October 30, 2026

3-Chloro-4-methoxybenzenesulfonamide → HCID 178464673, compound

https://huagongshe.com/reaction/1484437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-methoxybenzenesulfonamideHCID 967066—
ReactantHCID 67359253HCID 67359253—
SolventAcetonitrileHCID 6342—
ProductHCID 178464673HCID 17846467397%

Reaction Steps

0.75 g (1 mol equiv.) N-Ethyl-4,4-dimethyl-4,5-dihydro-pyrazole-1-carboximidothioic acid methyl ester and 0.94 g (1.05 mol equiv.) 3-chloro-4-methoxy-benzenesulfonamide were added to 10 mL acetonitrile. The reaction mixture was refluxed overnight and volatiles were removed in vacuo. The residue was taken up in ethyl acetate and extracted with 2N NaOH. The organic layer was dried over Na2SO4, filtered and evaporated to dryness. Purification by flash chromatography on silica gel (Et2O) afforded 1.43 g (97%) 3-chloro-N-[(4,4-dimethyl-4,5-dihydro-pyrazol-1-yl)-ethylamino-methylene]-4-methoxy-benzenesulfonamide. 1H NMR (400 MHz, CDCl3) δ 1.17 (t, J=7.3 Hz, 3H), 1.22 (s, 6H), 3.43-3.52 (m, 2H), 3.77 (br.s., 2H), 3.95 (s, 3H), 6.75 (s, 1H), 6.96 (d, J=8.6 Hz, 1H), 6.70-6.90 (br.s., 1H) 7.82 (dd, J=8.6, 2.3 Hz, 1H), 7.95 (d, J=2.3 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422244B2
Source datasetuspto-grants-2016_08
ORD IDord-1637e00ec13a46ac90cf43db5bd7c260
Source noteuspto-grants-2016_08