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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78383Erstellt: 25. Oktober 2026

4-Aminophenol → 4-Chloro-N-methylpicolinamide

https://huagongshe.com/reaction/78383

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-AminophenolHCID 403—
Edukt4-Chloro-N-methylpicolinamideHCID 1476814—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-Chloro-N-methylpicolinamideHCID 1476814—
Produkt4-(4-Aminophenoxy)-N-methylpicolinamideHCID 16655129—

Reaktionsschritte

Entry 103: 4-Chloro-N-methyl-2-pyridinecarboxamide was synthesized according to Method A2, Step 3b. 4-Chloro-N-methyl-2-pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 using DMAC in place of DMF to give 4-(2-(N-methylcarbamoyl)-4-pyridyloxy)aniline. According to Method C2b, reaction of 3-amino-2-methoxyquinoline with CDI followed by 4-(2-(N-methylcarbamoyl)-4-pyridyloxy)aniline afforded bis(4-(2-(N-methylcarbamoyl)-4-pyridlyoxy)phenyl)urea.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841330B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-2744b4db45e24ad68eba16d25b07aaea
Quellennotizuspto-grants-2014_09