HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133597Erstellt: 23. Oktober 2026
Diisopropylcarbodiimide → 4-[[N-(3-bromo-4-methylbenzoyl)glycyl]aminomethyl]-1-(4-chlorobenzyl)piperidine
https://huagongshe.com/de/reaction/133597
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylcarbodiimide | HCID 12734 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 3-Bromo-4-methylbenzoic acid | HCID 82130 | — |
| Edukt | 1-(4-Chlorobenzyl)-4-((glycylamino)methyl}piperidine | HCID 18426155 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | 4-[[N-(3-bromo-4-methylbenzoyl)glycyl]aminomethyl]-1-(4-chlorobenzyl)piperidine | HCID 18426237 | — |
Reaktionsschritte
3-Bromo-4-methylbenzoic acid (0.060 mmol), diisopropylcarbodiimide (0.060 mmol) and HOBt (0.060 mmol) were added to a solution of 1-(4-chlorobenzyl)-4-[(glycylamino)methyl]piperidine (0.050 mmol) in chloroform (1.35 mL) and tert-butanol (0.15 mL). The resulting reaction mixture was stirred at room temperature for 15 hours. The mixture was then loaded onto a Varian™ SCX column and washed with methanol/chloroform=1:1 (12 mL) and methanol (12 mL). The obtained crude product was eluted with a 2 M methanol solution of NH3 (5 mL) and concentrated to thereby afford 4-[[N-(3-bromo-4-methylbenzoyl)glycyl]aminomethyl]-1-(4-chlorobenzyl)piperidine (Compd. No. 1113) (16.1 mg, 65%). The purity was determined by RPLC/MS (95%). ESI/MS m/e 494.0 (C23H27BrClN3O2).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07390830B1 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-fac85c040d5049d0afcd61252ffa636f |
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| Quellennotiz | uspto-grants-2008_06 |
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