HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1500335Erstellt: 25. Oktober 2026
tert-Butyl methyl(3-oxopropyl)carbamate → Tert-butyl 3-(4-(dimethylamino)-4-phenylpiperidin-1-yl)propyl(methyl)carbamate
https://huagongshe.com/reaction/1500335
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butyl methyl(3-oxopropyl)carbamate | HCID 10442454 | — |
| Edukt | N,N-dimethyl-4-phenylpiperidin-4-amine dihydrochloride | HCID 67366566 | — |
| Edukt | CID 101953985 | HCID 101953985 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Chloroform methanol | HCID 21584188 | — |
| Produkt | Tert-butyl 3-(4-(dimethylamino)-4-phenylpiperidin-1-yl)propyl(methyl)carbamate | HCID 68494485 | — |
Reaktionsschritte
11.1 g (1.3 eq) tert-butyl methyl(3-oxopropyl)carbamate were added to a solution of 11 g (1 eq) N,N-dimethyl-4-phenylpiperidin-4-amine dihydrochloride in 110 ml methanol at 0° C. and the reaction mixture was stirred for 15 min at 0° C. 6.2 g (3 eq) sodium cyanoboron hydride were then added in portions and the mixture was stirred for 30 min at room temperature. The reaction mixture obtained was adjusted to a pH of 5-6 with acetic acid and stirred for 12 h at room temperature. The reaction course was monitored by thin-layer chromatography (20% MeOH/CHCl3). As the conversion was still not complete, 2.4 g sodium cyanoboron hydride were added and the reaction mixture obtained was adjusted to pH 5-6 with acetic acid and stirred for 60 min at room temperature.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09206156B2 |
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| Quelldatensatz | uspto-grants-2015_12 |
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| ORD ID | ord-f48332a52b454c169cd377fc55151a00 |
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| Quellennotiz | uspto-grants-2015_12 |
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