HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64333Erstellt: 24. Oktober 2026
N,N'-Dimethylethylenediamine → HCID 178513489, Verbindung
https://huagongshe.com/de/reaction/64333
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Edukt | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Edukt | 5-Amino-1-(2-bromo-5-nitrophenyl)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide | HCID 117668233 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 178513489 | HCID 178513489 | 52% |
Reaktionsschritte
A mixture of 5-amino-1-(2-bromo-5-nitrophenyl)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide (149 mg, 0.3 mmol, crude), CuI (5.7 mg, 0.03 mmol), N1,N2-dimethylethane-1,2-diamine (3 mg, 0.03 mmol), K3PO4 (64 mg, 0.3 mol) in 15 mL of DMF was stirred at 60° C. under N2 for 5 hr, until TLC analysis showed that most of starting material was consumed. The reaction was cooled to RT. The solvent was removed under reduced pressure. The residue was chromatographed on 5 g of silica gel using DCM/MeOH (200/1 to 20/1) to afford 62 mg (52%) of 7-nitro-2-(4-phenoxyphenyl)-4H-benzo[4,5]imidazo[1,2-b]pyrazole-3-carboxamide as a tan solid. MS (ESI) m/e [M+1]+ 414.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09447106B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-0f8b7e8bbaa3476090c8dfdeb1cd92e4 |
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| Quellennotiz | uspto-grants-2016_09 |
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