HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218463Generated: October 29, 2026
Sodium Formate → 3-(1H-benzimidazol-2-yl)-1H-indazole-5-carboxaldehyde
https://huagongshe.com/reaction/218463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | 3-(1H-Benzo[D]imidazol-2-YL)-5-iodo-1H-indazole | HCID 135971798 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(1H-benzimidazol-2-yl)-1H-indazole-5-carboxaldehyde | HCID 135971797 | 37% |
Reaction Steps
3-(1H-benzimidazol-2-yl)-5-iodo-1H-indazole (500 mg, 1.39 mmol) was dissolved in DMF (5 mL), then Pd(PPh3)2Cl2 (24 mg, 0.034 mmol) and sodium formate (142 mg, 2.1 mmol) were added. The reaction mixture was put under vacuum and recharged with CO three times, then heated up to 90° C. for 4 hr. The mixture was diluted with EtOAc, washed with brine, dried and concentrated. The crude product was purified by flash chromatography to afford 3-(1H-benzimidazol-2-yl)-1H-indazole-5-carboxaldehyde (135 mg, 37%) as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198456B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-3c75f4f93bc749b98db430601a9902e9 |
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| Source note | uspto-grants-2012_06 |
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