HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloropyrimidine → tert-Butyl 4-(4-chloropyrimidin-2-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Reactant | 1-Boc-4-methylpiperazine | HCID 11401394 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-Butyl 4-(4-chloropyrimidin-2-yl)piperazine-1-carboxylate | HCID 46738270 | 56.9% |
Reaction Steps
To a suspension of 2,4-dichloropyrimidine (1.00 g, 6.71 mmol) in 13.4 mL of toluene was added 4-methyl-piperazine-1-carboxylic acid tert-butyl ester (1.34 g, 6.71 mmol). The reaction was heated to reflux overnight, then cooled to room temperature and concentrated in vacuo. The residue was taken up in 20 mL of water and extracted with ethyl acetate (2×40 mL). The combined organic layers were washed with brine (25 mL), then dried over sodium sulfate, filtered, and concentrated in vacuo to an off-white solid. Flash column chromatography (silica gel, gradient elution from 5% ethyl acetate-hexanes to 20% ethyl acetate-hexanes) yielded 1.14 g of the title compound (I-2a).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06995159B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-ecaa0ddc47c040cf8f7aea32f78f69bb |
| Source note | uspto-grants-2006_02 |