Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tributylamine | HCID 7622 | — |
| Edukt | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Edukt | 3-ethyl-1-phenyl-1H-indazol-6-amine hydrochloride | HCID 67449229 | — |
| Edukt | HCID 178524171 | HCID 178524171 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 178437917 | HCID 178437917 | — |
Reaktionsschritte
Into a 100-mL 3-necked round-bottom flask, was placed a solution of 3-ethyl-1-phenyl-1H-indazol-6-amine hydrochloride (300 mg, 1.10 mmol, 1.00 equiv) in N,N-dimethylformamide (30 mL), tributylamine (492 mg, 2.66 mmol, 2.50 equiv), 1H-benzo[d]imidazole-5-carboxylic acid (180 mg, 1.11 mmol, 1.00 equiv), 2-chloro-1-methylpyridinium iodide (330 mg, 1.29 mmol, 1.20 equiv). The resulting solution was stirred for 2 days at 100° C. in an oil bath. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (50:1). The resulting mixture was diluted with methanol (10 mL) and the solids were washed with diethyl ether (1×50 mL) to yield N-(3-ethyl-1-phenyl-1H-indazol-6-yl)-1H-benzo[d]imidazole-5-carboxamide as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822447B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-29a404dda10f4116845058069a887d7a |
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| Quellennotiz | uspto-grants-2014_09 |
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