HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1280964Erstellt: 23. Oktober 2026
Acetic Acid → (R)-3-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl}amino]-1-(4,5-methylenedioxy-2-nitrobenzyl)pyrrolidine
https://huagongshe.com/de/reaction/1280964
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 6-Nitro-1,3-benzodioxole-5-carboxaldehyde | HCID 12840 | — |
| 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-(4,5-methylenedioxy-2-nitrobenzyl)pyrrolidine | HCID 69212304 | — |
Reaktionsschritte
To a mixture of (R)-3-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl}amino]pyrrolidine (0.150 mmol), 4,5-methylenedioxy-2-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-(4,5-methylenedioxy-2-nitrobenzyl)pyrrolidine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06451842B1 |
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| Quelldatensatz | uspto-grants-2002_09 |
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| ORD ID | ord-46c22ecc114c441bb4604564edc82ea6 |
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| Quellennotiz | uspto-grants-2002_09 |
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