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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(3-Fluoro-4-hydroxyphenyl)boronic acidHCID 23005361—
Reactant3-bromo-5-nitro-1-trityl-1H-indazoleHCID 58946443—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product3-(3-fluoro-4-hydroxyphenyl)-5-nitro-1-trityl-1H-indazoleHCID 136387210—

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546404B2
Source datasetuspto-grants-2013_10
ORD IDord-c8a738d0ee364e4ba4c656f8f710cefe
Source noteuspto-grants-2013_10