HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484443Generated: October 30, 2026
HCID 61129737, compound → HCID 178464667, compound
https://huagongshe.com/reaction/1484443
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 61129737 | HCID 61129737 | — |
| Reactant | HCID 67359253 | HCID 67359253 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178464667 | HCID 178464667 | 83% |
Reaction Steps
3.41 g (1 mol equiv.) N-Ethyl-4,4-dimethyl-4,5-dihydro-pyrazole-1-carboximidothioic acid methyl ester and 6.24 g (1.05 mol equiv.) N-(2-Bromo-4-sulfamoyl-phenyl)-2,2,2-trifluoro-acetamide were added to 100 mL acetonitrile. The reaction mixture was refluxed overnight, and subsequently volatiles were removed under reduced pressure. The residue was taken up in ethyl acetate and extracted with 2N NaOH, and the organic layer was dried over Na2SO4, filtered and evaporated to dryness. Purification by flash chromatography on silica gel (Et2O) afforded 7.1 g (83%) N-(2-bromo-4-{[(4,4-dimethyl-4,5-dihydro-pyrazol-1-yl)-ethylamino-methylene]-sulfamoyl}-phenyl)-2,2,2-trifluoro-acetamide. 1H NMR (400 MHz, CDCl3) δ 1.18 (t, J=7.3 Hz, 3H), 1.24 (s, 6H), 3.43-3.51 (m, 2H), 3.79 (br.s., 2H), 6.78 (s, 1H), 7.93 (dd, J=8.6, 2.0 Hz, 1H), 8.19 (d, J=2.0 Hz, 1H), 8.39 (d, J=8.6 Hz, 1H), 8.61 (br.s., 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-7a47d23b32144387a51f15975c4879dc |
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| Source note | uspto-grants-2016_08 |
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