HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77102Erstellt: 24. Oktober 2026
N,1-dimethylpyrrolidin-3-amine → HCID 178480456, Verbindung
https://huagongshe.com/de/reaction/77102
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N,1-dimethylpyrrolidin-3-amine | HCID 2758520 | — |
| Edukt | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Edukt | HCID 178479749 | HCID 178479749 | — |
| Produkt | HCID 178480456 | HCID 178480456 | 30% |
Reaktionsschritte
Method J—Step a To a mixture of 1-[3-(5-Chloro-1H-benzoimidazol-2-yl)-4-fluoro-phenyl]-piperidine-4-carboxylic acid hydrochloride (obtained as described in general method 10, step b) (0.01 g, 0.25 mmol) in dcm (2 mL), HATU (0.10 g, 0.26 mmol), TEA (0.07 mL, 0.55 mmol) and N,N′-dimethyl-3-aminopyrrolidine (0.04 g, 0.31 mmol) were added. The reaction mixture was heated at 35° C. overnight, cooled to room temperature and washed with ammonium chloride solution (2 mL), saturated Na2CO3 solution (2 mL) and water (2 mL). The organic layer was then filtrated on an NH2 cartridge and further purified by flash chromatography (eluent: EtOAc:NH3 2N in MeOH/9:1) to obtain 0.03 g of the title compound (30%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835648B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-5a847595c8984844a698703d86c9781a |
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| Quellennotiz | uspto-grants-2014_09 |
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