HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → tert-Butyl 4-(5-methylpyridin-2-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 5-Chloro-2-methylpyridine | HCID 2762869 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-Butyl 4-(5-methylpyridin-2-yl)piperazine-1-carboxylate | HCID 45788994 | — |
Reaction Steps
Under an argon atmosphere, 2.50 g (19.6 mmol) of 2-methyl-5-chloropyridine and 4.38 g (23.5 mmol) of N-(tert-butyloxycarbonyl)-piperazine are dissolved in 50 ml of absolute toluene. Then, 2.26 g (23.5 mmol) of sodium-tert-butylate, 0.37 g (0.59 mmol) of BINAP, and 0.36 g (0.39 mmol) of tris(dibenzylideneacetone)-dipalladium are added, and it is heated for 12 hours to 70° C. After cooling, the reaction mixture is mixed with diethyl ether, washed three times with saturated sodium chloride solution, dried on sodium sulfate, and solvent is removed in a vacuum. The residue is purified by flash chromatography (cyclohexane/ethyl acetate 9:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133165B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-eca7c9f093d4463fa5a7b6399bc4194f |
| Source note | uspto-grants-2015_09 |