HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361066Generated: October 25, 2026
Cesium carbonate → N-(4-(3-bromopyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine
https://huagongshe.com/reaction/2361066
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-((4-Phenylphthalazin-1-yl)amino)phenol | HCID 2869168 | — |
| Reactant | 3-Bromo-4-chloropyridine hydrochloride | HCID 46941422 | — |
| Product | N-(4-(3-bromopyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine | HCID 66731439 | — |
Reaction Steps
A resealable reaction tube was charged with cesium carbonate (0.873 g, 0.268 mmol), 3-bromo-4-chloropyridine hydrochloride (0.205 g, 0.894 mmol) and 4-(4-phenylphthalazin-1-ylamino)phenol (0.280 g, 0.894 mmol) and purged with nitrogen for several minutes. 1.8 mL of DMSO was added, the tube was sealed, and the reaction mixture was heated to 130° C. for 3 h. Upon cooling the mixture was diluted with EtOAc and washed with water. The aqueous portion was extracted with EtOAc, and the combined organic portions were dried with MgSO4 and concentrated. N-(4-(3-bromopyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine was isolated as an orange solid. MS m/z=470 [M+H]+. Calc'd for C25H17BrN4O: 469.33.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686155B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-f5670021cc254d25b310391fb240d536 |
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| Source note | uspto-grants-2014_04 |
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