HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → tert-Butyl4-(3-cyano-2-pyridinyl)-1-piperazinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloronicotinonitrile | HCID 81079 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-Butyl4-(3-cyano-2-pyridinyl)-1-piperazinecarboxylate | HCID 22061422 | — |
Reaction Steps
A mixture of 2-chloro-3-cyanopyridine (15.2 g, 0.11 mol), tert-butyl 1-piperazinecarboxylate (25 g, 0.13 mol) and triethylamine (18 ml, 0.13 mol) in toluene (200 ml), was heated under reflux for 24 hours. The cooled mixture was concentrated under reduced pressure and the residue suspended in ethyl acetate (250 ml), and washed with water (3×). The organic solution was dried (MgSO4), and concentrated under reduced pressure. The residue was triturated with pentane, filtered and dried in vacuo, at 60° C., to afford the title compound as a cream coloured solid, 24.2 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060836B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-4170c0f4d1d74f3ab1306d06b36dbb36 |
| Source note | uspto-grants-2006_06 |