HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloropyrimidine → Tert-butyl 4-(2-chloropyrimidin-4-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Tert-butyl 4-(2-chloropyrimidin-4-yl)piperazine-1-carboxylate | HCID 11197306 | — |
Reaction Steps
A mixture of 9.55 g of tert-butyl 1-piperazinecarboxylate, 7.64 g of 2,4-dichloropyrimidine and 8.6 g of NaHCO3 in 50 ml of EtOH is heated at reflux for 1 hour. It is concentrated under vacuum, the residue is taken up in water and extracted with DCM, the organic phase is dried over Na2SO4 and the solvent is evaporated under vacuum. The residue is chromatographed on silica gel, eluting with a DCM/AcOEt (90/10 to 60/40; v/v) mixture. Two compounds are separated:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468368B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-9500ad0063f54084b120d9d9ec5dc024 |
| Source note | uspto-grants-2008_12 |