HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75210Generated: October 27, 2026
Acetic Acid → 2-(3,5-dichloropyridin-4-yl)imidazo[4,5-d]dipyrido[2,3-b:3',4'-f]azepin-3(8H)-ol
https://huagongshe.com/reaction/75210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 3,5-Dichloro-4-pyridinecarboxaldehyde | HCID 2762988 | — |
| Reactant | HCID 178516817 | HCID 178516817 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-(3,5-dichloropyridin-4-yl)imidazo[4,5-d]dipyrido[2,3-b:3',4'-f]azepin-3(8H)-ol | HCID 66886986 | — |
Reaction Steps
5H-Dipyrido[2,3-b:3′,4′-f]azepine-5,6(11H)-dione 6-oxime (0.100 g, 0.416 mmol, Intermediate D-7) ammonium acetate (0.60 g, 8.0 mmol), acetic acid (2 mL), water (0.2 mL) and 3,5-dichloroisonicotinaldehyde (0.293 g, 1.66 mmol) were combined in a capped vial and heated to 80° C. for 2 h. The mixture was cooled to room temperature, and diluted with aqueous NaHCO3 and brine. The mixture was extracted three times with ethyl acetate and the combined extracts were washed with brine, dried over MgSO4, filtered, and concentrated to provide the crude intermediate product as a dark oil which was used directly in the next step. LC/MS: 397, 399 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835423B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a02a1e63cc8247c9ac115423ea9de726 |
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| Source note | uspto-grants-2014_09 |
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