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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33756Erstellt: 23. Oktober 2026

4-Aminobenzoic Acid → Benzimidazole

https://huagongshe.com/de/reaction/33756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Aminobenzoic AcidHCID 978—
EduktAnilineHCID 6115—
EduktCyanoacetamideHCID 7898—
EduktThiophosgeneHCID 10040—
EduktHCID 178418790HCID 178418790—
ProduktBenzimidazoleHCID 5798—
ProduktBenzothiazoleHCID 7222—
ProduktBenzenamine, 4-(2-benzoxazolyl)-HCID 88733—
ProduktThiocarbamoyl cyanoacetamideHCID 13573014—

Reaktionsschritte

The 2-(4-aminophenyl)benzoxazole, benzothiazole, or benzimidazole was prepared by condensation of the appropriate aniline derivative with p-amino benzoic acid using polyphosphoric acid. The product was converted to the corresponding isothiocyanate with thiophosgene and subsequently condensed with cyanoacetamide to form the thiocarbamoyl cyanoacetamide. Treatment with bromine afforded the cyano hydroxy thiazole, which was converted to carboxamidine by treatment with the appropriate amide, as shown above.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429667B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-ffad715435b24c70909bdbc409e32c04
Quellennotizuspto-grants-2008_09