HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727062Generated: October 30, 2026
1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride → HCID 57917724, compound
https://huagongshe.com/reaction/1727062
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride | HCID 2734913 | — |
| Reactant | 2-Bromo-5-(trifluoromethyl)pyridine | HCID 2736434 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 1189435-14-0 | HCID 67045962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57917724 | HCID 57917724 | 282.5% |
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-i-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07494999B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-08c9ffc9d829478e8a92ed887acff5bb |
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| Source note | uspto-grants-2009_02 |
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