HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378291Erstellt: 25. Oktober 2026
Triethylamine → N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide
https://huagongshe.com/reaction/378291
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methylamine hydrochloride | HCID 6364545 | — |
| Edukt | N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide | HCID 19353544 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide | HCID 17774522 | 43,8% |
Reaktionsschritte
0.36 g (0.0011 mol) of N-(6-chloro-2-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide was dissolved in 10 ml of ethanol, treated with 1.2 g (0.018 mol) of methylamine hydrochloride and 4.0 ml (0.029 mol) of triethylamine and stirred in an autoclave at 140° C. for 17 hours. The mixture was freed completely from solvent, the residue was partitioned in ethyl acetate/water, the insoluble constituents were filtered off under suction and extracted. The extract and the solid were combined and recrystallized from methanol/diethyl ether. There was obtained 0.15 g (43%) of N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-fluoro-benzenesulfonamide as white crystals; m.p. 261-263° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06030976 |
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| Quelldatensatz | uspto-grants-2000_02 |
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| ORD ID | ord-e43e829c2ce54c36ab02dad425a4882b |
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| Quellennotiz | uspto-grants-2000_02 |
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