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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465716Generated: October 31, 2026

Potassium Phosphate, Tribasic → HCID 67518058, compound

https://huagongshe.com/reaction/1465716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 67027251HCID 67027251—
ReactantHCID 67518406HCID 67518406—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67518058HCID 6751805830.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To tert-butyl 3-(4-bromo-1H-pyrazol-1-yl)piperidine-1-carboxylate (0.66 g, 2 mmol) and 3-(pyridin-4-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-trityl-1H-indazole (1.13 g, 2 mmol) in dioxane (8 mL) and water (2 mL) was added potassium phosphate (848 mg, 4 mmol) and PdCl2(dppf) (120 mg, 0.16 mmol). The reaction mixture was stirred at 80° C. for 24 h. After filtered through a pad of celite, and washed with EtOAc, the filtrate was washed with brine, dried and concentrated. The crude mixture was column purified with mixture of methanol, dichloromethane and ammonia to give tert-butyl 3-(4-(3-(pyridin-4-yl)-1-trityl-1H-indazol-5-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylate (420 mg) as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999966B2
Source datasetuspto-grants-2015_04
ORD IDord-c86f8c1d52f543c7885bc674ab237ee0
Source noteuspto-grants-2015_04