HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 239256Erstellt: 25. Oktober 2026
N-bromobutanimide → N-(3-(5-(2-chloro-4-pyrimidinyl)-2-(1,1-diethylethyl)-1,3-thiazol-4-yl)-2-fluoraphenyl)-2,6-difluorobenzenesulfonamide
https://huagongshe.com/reaction/239256
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 2,2-Dimethylpropanethioamide | HCID 3031130 | — |
| Edukt | N-(3-(2-(2-chloropyriMidin-4-yl)acetyl)-2-fluorophenyl)-2,6-difluorobenzenesulfonamide | HCID 57989720 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | N-(3-(5-(2-chloro-4-pyrimidinyl)-2-(1,1-diethylethyl)-1,3-thiazol-4-yl)-2-fluoraphenyl)-2,6-difluorobenzenesulfonamide | HCID 57989782 | — |
Reaktionsschritte
To a solution of N-{3-[(2-chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide (2.0 g, 4.53 mmol) in 40 mL DMA, 1.0 eq. NBS (0.806 g, 4.53 mmol) was added and the solution was allowed to stir 15 min at rt. 2,2-dimethylpropanethioamide (0.531 g, 4.53 mmol) was then added at rt. The reaction was heated to 60° C. for 2 hours. The reaction was not complete by LC-MS. The reaction mixture was then heated to 80° C. for an additional hour. The reaction mixture was diluted with water and extracted×2 with EtOAc. The combined EtOAc washings were washed with water×3 to remove DMA, dried over MgSO4, filtered and concentrated onto silica gel. The crude material was chromatographed in 10-80% EtOAc in Hexanes to give the desired product, 1.6 g (64%). MS (ESI): 539.1 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08642759B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-c39d8f945a7a41a09cbeaa053d72f205 |
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| Quellennotiz | uspto-grants-2014_02 |
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