HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68550Generated: October 29, 2026
Triethylamine → Tert-butyl 4-(6-methoxypyrimidin-4-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/68550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 4-Chloro-6-methoxypyrimidine | HCID 1051509 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 4-(6-methoxypyrimidin-4-yl)piperazine-1-carboxylate | HCID 66569709 | — |
Reaction Steps
18.6 mL triethylamine and piperazine-1-carboxylic acid tert-butyl ester were added to 9.7 g 4-chloro-6-methoxy-pyrimidine in 50 mL DMF. The reaction was stirred over night at 60° C. The reaction was cooled and the precipitate was filtered. The filtrate was evaporated. The residue was dissolved in DCM, extracted with water and washed with sodium chloride solution. The solvent was evaporated and the residue was crystallized with a mixture of petrolether and diethylether (8:2) to yield 8.7 g of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822464B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-480b9947a2fb41b6ab3655deb9dd0a1b |
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| Source note | uspto-grants-2014_09 |
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