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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727111Generated: November 2, 2026

Potassium Carbonate → HCID 57566680, compound

https://huagongshe.com/reaction/1727111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chlorophenylboronic acidHCID 2734322—
ReactantHCID 57566681HCID 57566681—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57566680HCID 5756668068.4%

Reaction Steps

To a solution of (Ph3P)4Pd (36 mg, 0.03 mmol) in dioxane ( 4 mL) under Argon was added 6-(2-Fluoro-phenoxy)-3-iodo-indazole-1-carboxylic acid tert-butyl ester (140 mg, 0.3 mmol) and the solution was stirred for 10 min, then 2-chlorophenyl boronic acid (96.4 mg, 0.6 mmol) in ethanol (1.2 mL) was added. After 10 min potassium carbonate (132 mg, 0.9 mmol) in water (0.4 mL) was added and the mixture was stirred at 85° C. under Argon for 18 h. The mixture was cooled to room temperature, filtered through Celite, partitioned between water and EtOAc, the separated organic phase was dried over Na2SO4 filtered, concentrated and the residue was purified by flash chromatography eluting with Hex:EtOAc 9:1 to yield 90 mg of 3-(2-Chloro-phenyl)-6-(2-fluoro-phenoxy)-indazole-1-carboxylic acid tert-butyl ester: MS: 345 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495015B2
Source datasetuspto-grants-2009_02
ORD IDord-c7f5e8d829154846a9f3116e83fc5ccf
Source noteuspto-grants-2009_02