HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252740Generated: October 31, 2026
Benzenesulfonamide → HCID 86620417, compound
https://huagongshe.com/reaction/252740
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 86244456 | HCID 86244456 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 86620417 | HCID 86620417 | 9.2% |
Reaction Steps
A mixture of N-[5-(6-chloropyridazin-4-yl)-4-methyl-1,3-thiazol-2-yl]acetamide (55 mg), benzenesulphonamide (49 mg), caesium carbonate (101 mg), cuprous iodide (30 mg) and DMA (1.5 mL) was heated in a microwave reactor to 200° C. under an argon atmosphere for 3 hours. The resultant mixture was evaporated and the residue was purified by preparative HPLC on reversed phase silica using a solvent gradient of 10% to 100% acetonitrile in water (containing 1% acetic acid) as eluent. The material so obtained was triturated under diethyl ether. There was thus obtained the title compound as a solid (7.3 mg); 1H NMR Spectrum: (DMSOd6+CD3CO2D) 2.20 (s, 3H), 2.43 (s, 3H), 7.51-7.64 (m, 3H), 7.75 (s, 1H), 7.89 (d, 2H), 8.51 (s, 1H); Mass Spectrum: M+H+ 390.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868188B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-66a61e56b6884bbcaa51cb7a692f5c95 |
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| Source note | uspto-grants-2011_01 |
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