HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16798Erstellt: 25. Oktober 2026
Trimethylaluminum → HCID 178489754, Verbindung
https://huagongshe.com/reaction/16798
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trimethylaluminum | HCID 16682925 | — |
| Edukt | Methyl 4-(1-cyclopropylpiperidin-4-yl)benzoate | HCID 57440413 | — |
| Edukt | HCID 178489815 | HCID 178489815 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | HCID 178489754 | HCID 178489754 | 35,8% |
Reaktionsschritte
Methyl 4-(1-cyclopropylpiperidin-4-yl)benzoate (0.259 g, 1 mmol), 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (0.247 g, 1.00 mmol) in toluene (10 ml) was treated with a 2M solution of trimethylaluminium (1.250 ml, 2.50 mmol) in toluene,under nitrogen. The reaction mixture was heated at 60° C. for 18 h. The reaction mixture was cooled and the reaction quenched with methanol (40 ml) and acidified with 2N HCl (1 ml). The crude reaction mixture was purified by ion exchange chromatography, using an SCX column. The crude product was eluted from the column using 7M NH3/MeOH and fractions were evaporated to dryness. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 5% 2.5M ammonia/methanol in DCM. Pure fractions were evaporated to dryness and the product crystallised from DCM/diethyl ether to give the title compound (0.170 g, 35.8%) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737149B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-5a9b645378f44bd8ae4503f944defaf2 |
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| Quellennotiz | uspto-grants-2010_06 |
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