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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1371789Erstellt: 26. Oktober 2026

4-Fluoro-3-methylanisole → (4-Amino-2-ethylsulfanyl-pyrimidin-5-yl)-(3-fluoro-6-methoxy-2-methyl-phenyl)-methanone

https://huagongshe.com/reaction/1371789

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Fluoro-3-methylanisoleHCID 137546—
Edukt5-Pyrimidinecarboxamide, 4-amino-2-(ethylthio)-N-methoxy-N-methyl-HCID 11974832—
Produkt(4-Amino-2-ethylsulfanyl-pyrimidin-5-yl)-(3-fluoro-6-methoxy-2-methyl-phenyl)-methanoneHCID 21070580—
Produkt(4-Amino-2-ethylsulfanyl-pyrimidin-5-yl)-(5-fluoro-2-methoxy-4-methyl-phenyl)-methanoneHCID 21070589—

Reaktionsschritte

The same procedure as described in Example 170 was used, starting from 4-amino-2-ethylsulfanyl-pyrimidine-5-carboxylic acid methoxy-methyl-amide (Example 1) and 4-fluoro-3-methylanisole (Aldrich), to give (4-amino-2-ethylsulfanyl-pyrimidin-5-yl)-(5-fluoro-2-methoxy-4-methyl-phenyl)-methanone as a white solid, MS (M+H)+, 322 and (4-amino-2-ethylsulfanyl-pyrimidin-5-yl)-(3-fluoro-6-methoxy-2-methyl-phenyl)-methanone as a white solid, MS (M+H)+, 322

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157455B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-207c35ad82344074a19d3c35eaebb959
Quellennotizuspto-grants-2007_01