HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484456Generated: November 2, 2026
(1E)-2-Phenylethenesulfonamide → HCID 178464676, compound
https://huagongshe.com/reaction/1484456
Participants
| Role | Name | HCID | Charge |
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| Reactant | (1E)-2-Phenylethenesulfonamide | HCID 5357731 | — |
| Reactant | HCID 67359394 | HCID 67359394 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178464676 | HCID 178464676 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422244B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-89cedf6493644fc1b9e502d3aea7e810 |
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| Source note | uspto-grants-2016_08 |
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