HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323149Erstellt: 23. Oktober 2026
Methylamine → 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-methylaminomethylphenyl)benzamide
https://huagongshe.com/de/reaction/323149
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methylamine | HCID 6329 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamide | HCID 22010987 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-methylaminomethylphenyl)benzamide | HCID 22010845 | — |
Reaktionsschritte
A mixture of 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamide (150 mg), methylamine (38% in methanol, 0.5 ml) and 3 Å molecular sieves (500 mg) in methanol (10 ml) was stirred at ambient temperature overnight. Sodium borohydride (39 mg) was added to the solution and the mixture was stirred at ambient temperature for 4 hours. The mixture was diluted with chloroform and the solution was washed with saturated aqueous sodium hydrogen carbonate and brine. The organic phase was dried over magnesium sulfate and the solvent was evaporated in vacuo to give crude oil. The oil was purified by silica gel column (10 g, 2% methanol in chloroform) and the product was solidified with diethyl ether to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-methylaminomethylphenyl)benzamide (160 mg) as a white powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06211242B1 |
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| Quelldatensatz | uspto-grants-2001_04 |
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| ORD ID | ord-9bf97a0e09ea4ddabf3692a82a27474d |
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| Quellennotiz | uspto-grants-2001_04 |
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