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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33756Generated: October 23, 2026

4-Aminobenzoic Acid → Benzimidazole

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzoic AcidHCID 978—
ReactantAnilineHCID 6115—
ReactantCyanoacetamideHCID 7898—
ReactantThiophosgeneHCID 10040—
ReactantHCID 178418790HCID 178418790—
ProductBenzimidazoleHCID 5798—
ProductBenzothiazoleHCID 7222—
ProductBenzenamine, 4-(2-benzoxazolyl)-HCID 88733—
ProductThiocarbamoyl cyanoacetamideHCID 13573014—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429667B2
Source datasetuspto-grants-2008_09
ORD IDord-ffad715435b24c70909bdbc409e32c04
Source noteuspto-grants-2008_09