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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-4-methoxybenzenesulfonamide | HCID 967066 | — |
| Reactant | HCID 67359253 | HCID 67359253 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178464673 | HCID 178464673 | 97% |
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
| 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-1637e00ec13a46ac90cf43db5bd7c260 |
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| Source note | uspto-grants-2016_08 |
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