HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68693Erstellt: 25. Oktober 2026
Cesium carbonate → 3-ethyl-1-phenyl-1H-indazol-6-amine
https://huagongshe.com/reaction/68693
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | Benzophenone imine | HCID 136809 | — |
| Edukt | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Edukt | 6-bromo-3-ethyl-1-phenyl-1H-indazole | HCID 67449468 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-ethyl-1-phenyl-1H-indazol-6-amine | HCID 67449230 | — |
Reaktionsschritte
Into a 100-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 6-bromo-3-ethyl-1-phenyl-1H-indazole (300 mg, 1.00 mmol, 1.00 equiv) in tetrahydrofuran (30 mL), Xantphos (64 mg, 0.11 mmol, 0.11 equiv), Pd(OAc)2 (33 mg, 0.15 mmol, 0.15 equiv), Cs2CO3 (214 mg, 1.11 mmol, 1.11 equiv), diphenylmethanimine (200 mg, 1.10 mmol, 1.10 equiv). The resulting solution was heated to reflux for 16 h in an oil bath. The resulting mixture was concentrated under vacuum. The residue was dissolved in tetrahydrofuran/3N hydrogen chloride (15 mL/5 mL). The resulting solution was stirred for an additional 2 h at room temperature, then concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate:MeOH:NH4OH (30:1:0.3) to yield 3-ethyl-1-phenyl-1H-indazol-6-amine as yellow oil.
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-0be362da01f74ee180311003e9d2e7ed |
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| Quellennotiz | uspto-grants-2014_09 |
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