HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279270Erstellt: 24. Oktober 2026
Acetic Acid → (R)-3-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl}amino]-1-(4-chloro-3-nitrobenzyl)pyrrolidine
https://huagongshe.com/de/reaction/279270
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 4-Chloro-3-nitrobenzaldehyde | HCID 85505 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | (R)-3-[[N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl]amino]pyrrolidine | HCID 54307129 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (R)-3-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl}amino]-1-(4-chloro-3-nitrobenzyl)pyrrolidine | HCID 54097878 | — |
Reaktionsschritte
To a mixture of (R)-3-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl}amino]pyrrolidine (0.150 mmol), 4-chloro-3-nitrobenzaldehyde (0.45 mmol), methanol (4.5 mL), and acetic acid (0.048 mL) was added NaBH3CN (0.75 mmol) in methanol (1.50 mL). The reaction mixture was stirred at 50° C. overnight. The mixture was cooled to room temperature, loaded onto Varian™ SCX column, and washed with CH3OH. Product was eluted off using 2 N NH3 in CH3OH and concentrated to afford (R)-3-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl}amino]-1-(4-chloro-3-nitrobenzyl)pyrrolidine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06362177B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-99f29f33ef3f429abc6fdfee499bb90d |
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| Quellennotiz | uspto-grants-2002_03 |
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