HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 1,1-Dimethylethyl 4-(5-iodo-2-pyrazinyl)-1-piperazinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 2-Bromo-5-iodopyrazine | HCID 21931200 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1,1-Dimethylethyl 4-(5-iodo-2-pyrazinyl)-1-piperazinecarboxylate | HCID 86669229 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
2-bromo-5-iodopyrazine (503 mg, 1.77 mmol) and tert-butyl piperazine-1-carboxylate (355 mg, 1.91 mmol) were taken up in tBuOH (8 mL). iPr2NEt (400 μL, 2.3 mmol) was added and the stirred reaction mixture was heated to 100° C. After 66 h, the reaction mixture was cooled and was partitioned between EtOAc, water and brine. The phases were separated, and the organic phase was dried over Na2SO4, filtered, and concentrated. The crude residue was purified by silica gel chromatography (10-30% EtOAc in hexanes) to afford tert-butyl 4-(5-iodopyrazin-2-yl)piperazine-1-carboxylate 7.11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09376441B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-a53a06b1ed774fd19e6d7b53c443e10b |
| Source note | uspto-grants-2016_06 |