HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1185444Erstellt: 26. Oktober 2026
1-Piperazinecarboxylic acid, ethyl ester → 4-((S)-2-benzyloxycarbonylamino-3-tert-butoxycarbonyl-propionyl)-piperazine-1-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1185444
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Piperazinecarboxylic acid, ethyl ester | HCID 8431 | — |
| Edukt | 4-tert-Butyl hydrogen N-((phenylmethoxy)carbonyl)-L-aspartate | HCID 111082 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | O-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733286 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-((S)-2-benzyloxycarbonylamino-3-tert-butoxycarbonyl-propionyl)-piperazine-1-carboxylic acid ethyl ester | HCID 66920269 | — |
Reaktionsschritte
To a solution of 25 g of (S)-2-Benzyloxycarbonylamino-succinic acid 4-tert-butyl ester, 35.6 g of NEM and 25.3 g of TOTU in 125 ml of DMF, 12.9 g of Piperazine-1-carboxylic acid ethyl ester was added at RT and stirred for 3 h. The reaction mixture was diluted saturated aqueous sodium hydrogen carbonate solution and extracted with 400 ml of ethyl acetate. The organic phase was washed with diluted saturated aqueous sodium hydrogen carbonate solution and dried over MgSO4 and the solvents were removed under reduced pressure. The crude product was purified by chromatography on silica gel eluting with n-heptane/ethyl acetate (1/1). The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 35.4 g.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08669266B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-a353c04b1cfd4b909f7c6f2e9469fe64 |
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| Quellennotiz | uspto-grants-2014_03 |
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