HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-1-Boc-3-methylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (R)-1-Boc-2-tert-butyl-3-methyl-4-imidazolidinone | HCID 546472 | — |
| Reactant | 2-Methylpiperazine, (S)- | HCID 2734219 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (S)-1-Boc-3-methylpiperazine | HCID 7023035 | — |
Reaction Steps
1-(tert-butoxycarbonyl)-2-tert-butyl-3-methyl-4-imidazolidinone (2 g, 8.3 mmol) (BOC—ON), in chloroform (15 ml), was added to (2S)-2-methylpiperazine (5 g, 50 mmol), a compound of formula (A), in a mixture of triethylamine (1.25 g, 12.5 mmol) and chloroform. The mixture was stirred for about 15 hours and then washed with water, the solvent removed in vacuo. The residue was purified by column chromatography, to give tert-butyl (3S)-3-methylpiperazinecarboxylate, a compound of formula (B).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06849632B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-182168b7a48648cf91d58092eaab5d2c |
| Source note | uspto-grants-2005_02 |