HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404680Generated: October 31, 2026
2-Pyridinecarboxaldehyde → HCID 178419322, compound
https://huagongshe.com/reaction/1404680
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Reactant | 4-Bromobenzene-1,2-diamine | HCID 323593 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178419322 | HCID 178419322 | 40.5% |
Reaction Steps
A mixture of 4-bromo-1,2-diaminobenzene (1.00 g, 5.35 mmol), sodium bisulfite (1.02 g) in water (8 mL) and ethanol (80 mL) and 2-pyridine carboxaldehyde (0.63 g, 5.88 mmol) was heated at 90° C. for 15 h. The reaction was cooled to room temperature and concentrated under vacuum. The residue was partitioned between water (60 mL) and chloroform (80 mL) and the aqueous phase was extracted with chloroform (2×50 mL). The organic extracts were combined, dried (MgSO4), filtered and concentrated under vacuum to give the crude product (1.36 g). The residue was purified by column chromatography eluting with EtOAc:hexaxes 0 to 50% to afford 594 mg of 5-bromo-2-(pyridin-2-yl)-1H-benzo[d]imidazole (40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08912336B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-38ac2725cbc2442bb6994e4bdaa5c35c |
|---|
| Source note | uspto-grants-2014_12 |
|---|