HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopyridine → (S)-tert-butyl 2-methyl-4-(pyridin-2-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl (2S)-2-methylpiperazine-1-carboxylate | HCID 10081508 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (S)-tert-butyl 2-methyl-4-(pyridin-2-yl)piperazine-1-carboxylate | HCID 70665341 | 47% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To a solution of tert-butyl (2S)-2-methylpiperazine-1-carboxylate (8 g, 39.94 mmol) in DMSO (25 ml) was added 2-bromopyridine (6.594 g, 41.74 mmol), and DIEA (15.48 g, 119.78 mmol). After stirring 2 days at 120° C., the resulting solution was quenched by the addition of DCM (200 ml), washed with water (3×300 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure to afford a residue, which was purified via silica gel chromatography (3% ethyl acetate in petroleum ether) to afford (S)-tert-butyl 2-methyl-4-(pyridin-2-yl)piperazine-1-carboxylate as a red oil (5.2 g, 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912188B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-0eca1fcfc8ac4cda9fac2206d9eefbd9 |
| Source note | uspto-grants-2014_12 |