HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1584206Erstellt: 26. Oktober 2026
Triethylamine → N-(2,6-bis-methylamino-pyrimidin-4-yl)-3-chloro-benzenesulfonamide
https://huagongshe.com/reaction/1584206
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methylamine hydrochloride | HCID 6364545 | — |
| Edukt | 3-chloro-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide | HCID 19353559 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | N-(2,6-bis-methylamino-pyrimidin-4-yl)-3-chloro-benzenesulfonamide | HCID 17774520 | 41% |
Reaktionsschritte
0.10 g (0.00030 mol) of 3-chloro-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide was dissolved in 5 ml of EtOH, treated with 0.27 g (0.004 mol) of methylamine hydrochloride and 1 ml (0.007 mol) of triethylamine and stirred in an autoclave at 145° C. for 17 hours. The entire reaction mixture was partitioned in ethyl acetate/water and extracted. The residue was recrystallized from MeOH. There was obtained 0.04 g (41%) of N-(2,6-bis-methylamino-pyrimidin-4-yl)-3-chloro-benzenesulfonamide as white crystals; m.p. 167-168° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05932599 |
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| Quelldatensatz | uspto-grants-1999_08 |
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| ORD ID | ord-0f2516fe7f9d488995b5ba8e812c4f02 |
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| Quellennotiz | uspto-grants-1999_08 |
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