HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46326Erstellt: 23. Oktober 2026
Lithium Hexamethyldisilazide → 5-chloro-N-(2,4-dimethoxybenzyl)-2,4-difluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide
https://huagongshe.com/de/reaction/46326
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Edukt | 5-Chloro-2,4-difluorobenzenesulphonyl chloride | HCID 2773527 | — |
| Edukt | N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amine | HCID 57732216 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-chloro-N-(2,4-dimethoxybenzyl)-2,4-difluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide | HCID 59436614 | — |
Reaktionsschritte
To a solution of (N-(2,4-dimethoxybenzyl)-1,2,4-thiadiazol-5-amine (Preparation 14, 40.6 g, 0.1619 mol) in anhydrous tetrahydrofuran (600. mL), cooled to −70° C., under nitrogen was added lithium 1,1,1,3,3,3-hexamethyldisilazan-2-ide (1 M in tetrahydrofuran, 161.9 mL, 0.161.9 mol) drop wise. The reaction mixture was warmed to room temperature and stirred for 1 hour before cooling to −70° C. A solution of 5-chloro-2,4-difluorobenzenesulfonyl chloride (40 g, 0.1619 mol) in tetrahydrofuran (200.0 mL) was added dropwise. After complete addition, the reaction mixture was gradually warmed to room temperature and stirred for 1 hour. Reaction mixture was quenched with saturated aqueous ammonium chloride solution and extracted with ethyl acetate. Organic layer was washed with water and saturated aqueous sodium chloride solution. Crude residue was purified by column chromatography eluting with ethyl acetate:hexane (gradient 1:19 to 3:17, by volume) to afford the title compound as a white solid, 46 g.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541588B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-4ea339d1094b4716bee2f3fde194d6d2 |
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| Quellennotiz | uspto-grants-2013_09 |
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