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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484456Generated: November 2, 2026

(1E)-2-Phenylethenesulfonamide → HCID 178464676, compound

https://huagongshe.com/reaction/1484456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1E)-2-PhenylethenesulfonamideHCID 5357731—
ReactantHCID 67359394HCID 67359394—
SolventAcetonitrileHCID 6342—
ProductHCID 178464676HCID 17846467681%

Reaction Steps

0.70 g (1 mol equiv.) 4,N-Diethyl-4,5-dihydro-pyrazole-1-carboximidothioic acid methyl ester and 0.68 g (1.05 mol equiv.) trans-2-phenyl-ethenesulfonic acid amide were added to 7 mL acetonitrile, and the reaction mixture was refluxed overnight. Volatiles were removed under reduced pressure, and 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:PA=2:1) afforded 1.00 g (81%) trans-2-phenyl-ethenesulfonic acid ethylamino-(4-ethyl-4,5-dihydro-pyrazol-1-yl)-methyleneamide. 1H NMR (400 MHz, CDCl3) δ 0.98 (t, J=7.5 Hz, 3H), 1.21 (t, J=7.2 Hz, 3H), 1.46-1.70 (m, 2H), 3.06-3.16 (m, 1H), 3.51-3.59 (m, 2H), 3.74 (dd, J=11.3, 7.5 Hz, 1H), 4.13 (t, J=11.3 Hz, 1H), 6.70-6.92 (m, 1H), 6.92 (d, J=1.3 Hz, 1H), 6.97 (d, J=15.4 Hz, 1H), 7.35-7.41 (m, 3H), 7.44 (d, J=15.4 Hz, 1H), 7.46-7.50 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422244B2
Source datasetuspto-grants-2016_08
ORD IDord-89cedf6493644fc1b9e502d3aea7e810
Source noteuspto-grants-2016_08