HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038137Generated: November 1, 2026
Potassium Phosphate, Tribasic → 3-(3-fluoro-4-hydroxyphenyl)-5-nitro-1-trityl-1H-indazole
https://huagongshe.com/reaction/1038137
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | (3-Fluoro-4-hydroxyphenyl)boronic acid | HCID 23005361 | — |
| Reactant | 3-bromo-5-nitro-1-trityl-1H-indazole | HCID 58946443 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | 3-(3-fluoro-4-hydroxyphenyl)-5-nitro-1-trityl-1H-indazole | HCID 136387210 | — |
Reaction Steps
A suspension of 3-bromo-5-nitro-1-trityl-1H-indazole 1AJ (10.0 g, 20.68 mmol), 3-fluoro-4-hydroxyphenylboronic acid 2AW (3.55 g, 22.78 mmol), Pd(dppf)Cl2 (1.6 g, 1.96 mmol) and K3PO4 (10.6 g, 4.99 mmol) in 200 mL of dioxane/H2O (4/1) was heated to 75° C. for overnight. After removal of most of the solvent, the black residue was diluted with EtOAc (250 mL) and H2O (60 mL). The resulting mixture was filtered through a pad of Celite. Additional 150 mL of EtOAc was used to wash the Celite cake. The filtrates were combined. The aqueous layer was separated and the organic layer was washed with brine, dried (MgSO4) and concentrated to give a green solid, which was recrystallized from CH2Cl2/hexane to give 3-(3-fluoro-4-hydroxyphenyl)-5-nitro-1-trityl-1H-indazole 3AW (8.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546404B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-c8a738d0ee364e4ba4c656f8f710cefe |
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| Source note | uspto-grants-2013_10 |
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