HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38047Erstellt: 24. Oktober 2026
Diisopropylethylamine → (S)-3-((S)-2-Chloro-4-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl-benzenesulfonyl)-pyrrolidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/de/reaction/38047
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | (6S)-1,4-Diazabicyclo(4.3.0)nonane | HCID 781249 | — |
| Edukt | (S)-tert-butyl 3-(2-chloro-4-fluorophenylsulfonyl)-pyrrolidine-1-carboxylate | HCID 67496058 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | (S)-3-((S)-2-Chloro-4-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl-benzenesulfonyl)-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 67496771 | 96% |
Reaktionsschritte
In a 50 mL round-bottomed flask, (S)-tert-butyl 3-(2-chloro-4-fluorophenylsulfonyl)-pyrrolidine-1-carboxylate, example 52D) (2 g, 5.5 mmol, 1 eq) was combined with acetonitrile (20 mL) to give a light yellow solution. (S)-octahydropyrrolo[1,2-a]pyrazine (1.04 g, 8.25 mmol, 1.5 eq) and DIEA (1.42 g, 1.92 mL, 11.0 mmol, 2 eq) were added. The reaction mixture was stirred for 15 h. The reaction mixture was heated to 60° C. and stirred for 5 h. The crude reaction mixture was concentrated in vacuo. The reaction mixture was poured into EtOAc (25 mL) and extracted with aqueous 10% Na2CO3 (2×20 mL) and brine. The organic layers were dried over Na2SO4 and concentrated in vacuo to yield a colorless viscous oil (2.48 g, 96%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524710B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-09e4fc306dde4c99b057c29a538b6279 |
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| Quellennotiz | uspto-grants-2013_09 |
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