HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminobenzoic Acid → Benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminobenzoic Acid | HCID 978 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | HCID 178418790 | HCID 178418790 | — |
| Product | Benzimidazole | HCID 5798 | — |
| Product | Benzothiazole | HCID 7222 | — |
| Product | Benzenamine, 4-(2-benzoxazolyl)- | HCID 88733 | — |
| Product | Thiocarbamoyl cyanoacetamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429667B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-ffad715435b24c70909bdbc409e32c04 |
| Source note | uspto-grants-2008_09 |