HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 896334, compound → HCID 21449927, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 896334 | HCID 896334 | — |
| Reactant | HCID 1088934 | HCID 1088934 | — |
| Reactant | HCID 3532018 | HCID 3532018 | — |
| Reactant | HCID 21449941 | HCID 21449941 | — |
| Reactant | HCID 21449944 | HCID 21449944 | — |
| Product | HCID 21449927 | HCID 21449927 | — |
Reaction Steps
Substitution of an equivalent amount of other heterocyclic acid chlorides, e.g., pyridine 2-, 3-, and 4-carboxylic acid chlorides; thenoyl 2- and 3-chlorides, coumariloyl chloride for thiazole-4-carboxylic acid chloride provides a convenient synthesis for: 2-(pyridine-2-carboxamido)benzimidazole, 2-(pyridine-3-carboxamido)benzimidazole, 2-(pyridine-4-carboxamido)benzimidazole, 2-(thiophene-2-carboxamido)benzimidazole, 2-(coumariloyl)aminobenzimidazole, m.p. 293°- 295° C. λmax. 327 mμ, E11%cm. 1024 and 2-nicotinamidoaminobenzimidazole, λmax. 319 mμ, E1cm.1% 429.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04011236 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-e384fae7ff89423cb98656fac17c3c3e |
| Source note | uspto-grants-1977_03 |