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HRID 472096Erstellt: 25. Oktober 2026

Dimethylamine → 2-amino-5-bromo-N,N-dimethylpyridine-3-sulfonamide

https://huagongshe.com/reaction/472096

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
EduktPyridineHCID 1049—
EduktTetrahydrofuranHCID 8028—
Edukt2-Amino-5-bromopyridine-3-sulfonyl chlorideHCID 53302026—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-amino-5-bromo-N,N-dimethylpyridine-3-sulfonamideHCID 5233515355%

Reaktionsschritte

To a cold (0 C) suspension of 2-amino-5-bromo-3-pyridinesulfonyl chloride (92.1 mmol) in dry 1,4-dioxane (92 mL) was added pyridine (101.3 mmol) followed by a 2M solution of dimethylamine in THF (101.3 mmol). The reaction was allowed to warm to rt for 2 h, heated to 50 C for 1 h, then cooled to rt. After standing for 2 h, the precipitate was collected by filtration and rinsed with a minimal amount of cold water. Drying the precipitate to constant weight under high vacuum provided 14.1 g (55%) of the title compound as a white solid. MS (ES)+m/e 279.8, 282.0 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08633187B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-897a678f2067438d831a0eadeb4346b3
Quellennotizuspto-grants-2014_01