HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → 1-methyl-N-(4-{[4-(methylamino)-3-nitrophenyl]oxy}pyridin-2-yl)piperidine-4-carboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Edukt | 1-Methylpiperidine-4-carboxylic acid | HCID 2736939 | — |
| Edukt | [4-(2-Amino(4-pyridyloxy))-2-nitrophenyl]methylamine | HCID 69006232 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-methyl-N-(4-{[4-(methylamino)-3-nitrophenyl]oxy}pyridin-2-yl)piperidine-4-carboxamide | HCID 69003266 | — |
Reaktionsschritte
To a mixture of 1-methylpiperidine-4-carboxylic acid (1 eq) in N,N-dimethyl formamide and N,N-disopropylethylamine (4 eq) was added BOP (2 eq) and the mixture was stirred at ambient temperature until homogeneous. To it was added [4-(2-amino(4-pyridyloxy))-2-nitrophenyl]methylamine (1 eq) and the resulting mixture was stirred at 60° C. for 16 h. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was dried over sodium sulfate and the resulting 1-methyl-N-(4-{[4-(methylamino)-3-nitrophenyl]oxy}pyridin-2-yl)piperidine-4-carboxamide was purified by silica gel chromatography. MS: MH+=386.2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07423150B2 |
| Quelldatensatz | uspto-grants-2008_09 |
| ORD ID | ord-a174a43a92334bcdb6c395c164189f26 |
| Quellennotiz | uspto-grants-2008_09 |