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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110131Generated: October 31, 2026

2-Bromo-5-(trifluoromethyl)pyridine → HCID 57917724, compound

https://huagongshe.com/reaction/2110131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-(trifluoromethyl)pyridineHCID 2736434—
Reactant1,3-Bis(2,6-di-1-propylphenyl)imidazolium chlorideHCID 22314747—
ReactantSodium t-butoxideHCID 23676156—
Reactant1189435-14-0HCID 67045962—
SolventTolueneHCID 1140—
ProductHCID 57917724HCID 57917724282.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

3-Methyl-piperazine-1,3-dicarboxylic acid 1-tert-butyl ester (120 mg, 0.49 mmol) and 2-Bromo-5-trifluoromethyl-pyridine (133 mg, 0.59 mmol) were dissolved in 2.0 mL of anhydrous toluene (degassed). In a separate, septum-equipped vial were placed tri(dibenzylideneacetone)dipalladium (0) (22 mg, 0.024 mmol), 1,3-bis(2,6-di-1-propylphenyl)imidazolium chloride (42 mg, 0.1 mmol) and sodium t-butoxide (57 mg, 0.59 mmol). This “catalytic” vial was equipped with a magnetic stir bar and flushed with dry nitrogen. The reactant solution was next transferred to the “catalytic” vial and the mixture was stirred at 100° C. for 5 h. After this period the mixture was combined with 20 mL of hexane/EtOAc (2:1) and was passed through a pad of Celite. The resulting filtrate was evaporated in vacuo and purified using flash silica chromatography (0-20% EtOAc/Hexane) to yield 110 mg (58%) of 4-(5-Trifluoromethyl-pyridin-2-yl)-piperazine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517884B2
Source datasetuspto-grants-2009_04
ORD IDord-c2efb4c28c69433da6807e3a45eda2a4
Source noteuspto-grants-2009_04