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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2270746Erstellt: 25. Oktober 2026

2-Amino-5-methylpyridine → Thiophene-3-sulfonamide

https://huagongshe.com/reaction/2270746

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-5-methylpyridineHCID 15348—
Edukt1-(6-Amino-1,3-benzodioxol-5-yl)ethan-1-oneHCID 120000—
EduktN-(4-chloro-3-methyl-5-isoxazolyl)2-{[2-acetyl-4,5-(methylenedioxy)phenyl]aminocarbonyl}thiophene-3-sulfonamideHCID 10696210—
ProduktThiophene-3-sulfonamideHCID 1201388—
ProduktN-(4-chloro-3-methyl-5-isoxazolyl)-2-[(3-methyl-6-pyridyl)aminocarbonyl]thiophene-3-sulfonamideHCID 10740439—

Reaktionsschritte

N-(4-chloro-3-methyl-5-isoxazolyl)-2-(3-methyl-6-pyridyl)aminocarbonyl]thiophene-3-sulfonamide was prepared by the method set forth for N-(4-chloro-3-methyl-5-isoxazolyl) 2-{[2-acetyl-4,5-(methylenedioxy)-phenyl]aminocarbonyl}thiophene-3-sulfonamide (EXAMPLE 148), except that 2-amino-5-picoline was used in stead of 2′-amino-4′,5′-(methylenedioxy)acetophenone, N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(3-methyl-6-pyridyl)aminocarbonyl]thiophene-3-sulfonamide was obtained, via HPLC purification of the crude reaction mixture, as a bright yellow powder (17% yield, m.p. 158-160° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06331637B1
Quelldatensatzuspto-grants-2001_12
ORD IDord-ee0d6b9e1226458c9a3cbd5162ef7550
Quellennotizuspto-grants-2001_12