HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Benzimidazolecarboxylic acid → 6-(1H-Benzo[d]imidazol-6-yl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Benzimidazolecarboxylic acid | HCID 459456 | — |
| Reactant | HCID 178488244 | HCID 178488244 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | 6-(1H-Benzo[d]imidazol-6-yl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole | HCID 24954872 | 17.5% |
Reaction Steps
A mixture of 4-amino-3-mercapto-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazole (80 mg, 0.28 mmol) and 3H-benzo[d]imidazole-5-carboxylic acid (46 mg, 0.28 mmol) in phosphoryl chloride (2 mL) was refluxed for 3 h. The solvent was evaporated and the residue was dissolved in dichloromethane (20 mL). It was neutralized with aqueous sodium carbonate. The organic layer was dried over sodium sulfate, concentrated to give 20 mg (17%) of the title compound as a solid. 1H NMR (CD3OD): 8.55 (s, 1H), 8.35 (s, 1H), 8.01-7.85 (m, 2H), 7.72 (s, 1H), 3.99 (s, 6H), 3.87 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732468B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-33ed9116bcc6491594f2303dbec72685 |
| Source note | uspto-grants-2010_06 |