HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11350Erstellt: 25. Oktober 2026
tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl 4-[(2-chloro-6-methyl-3-nitropyridin-4-yl)amino]butylcarbamate
https://huagongshe.com/reaction/11350
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| Edukt | 2,4-Dichloro-6-methyl-3-nitropyridine | HCID 2784819 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Tert-butyl 4-[(2-chloro-6-methyl-3-nitropyridin-4-yl)amino]butylcarbamate | HCID 12109135 | 98,5% |
Reaktionsschritte
A solution of tert-butyl 4-aminobutylcarbamate (32.12 g, 170.6 mmol) in N,N-dimethylformamide (200 mL) was added over a period of 90 minutes to a solution of 2,4-dichloro-6-methyl-3-nitropyridine (35.09 g, 169.5 mmol) in N,N-dimethylformamide (500 mL). The reaction mixture was stirred at ambient temperature overnight. The solvent was removed by vacuum distillation using a 24/40 short path distillation head and warm water. The residue was dissolved in ethyl acetate (700 mL), washed with water (3×100 mL), dried over magnesium sulfate and then concentrated under reduced pressure. The crude product was purified by column chromatography (50×450 mm silica gel eluting with 1:1 hexane:ethyl acetate) to provide 59.90 g of tert-butyl 4-[(2-chloro-6-methyl-3-nitropyridin-4-yl)amino]butylcarbamate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07098221B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-fded4986a54d42f184599c02d1ee8017 |
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| Quellennotiz | uspto-grants-2006_08 |
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