HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324781Erstellt: 25. Oktober 2026
3,4-Dichlorobenzaldehyde → 3-Phenylpropyl 4-(3,4-dichlorophenyl)-2-phenyl-6-[(2-(1-piperidinyl)ethoxy)methyl]-1,4-dihydropyrimidine-5-carboxylate
https://huagongshe.com/reaction/324781
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3,4-Dichlorobenzaldehyde | HCID 22710 | — |
| Edukt | Benzamidine, hydrochloride | HCID 80289 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | 3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate | HCID 22005512 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-Phenylpropyl 4-(3,4-dichlorophenyl)-2-phenyl-6-[(2-(1-piperidinyl)ethoxy)methyl]-1,4-dihydropyrimidine-5-carboxylate | HCID 22005530 | 2,3% |
Reaktionsschritte
A mixture of 3-phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate (1.50 g, 4.32 mmol), 3,4-dichlorobenzaldehyde (0.907 g, 5.18 mmol), benzamidine hydrochloride (0.811 g, 5.18 mmol) and sodium acetate (0.425 g, 5.18 mmol) was stirred in N,N-dimethylformamide (10 mL) for 14 days at room temperature and then heated to 60° C. for 3 days. The DMF was removed in vacuo and ethyl acetate was added to the residue. The precipitate was removed by filtration and the filtrate was washed with water, sodium hydrogen carbonate solution and brine, dried and evaporated to yield an oil. The oil was further purified by flash chromatography and RP-HPLC to give the title compound (60 mg) as an oil. Electrospray MS m/z 606/608 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06218538B1 |
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| Quelldatensatz | uspto-grants-2001_04 |
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| ORD ID | ord-ae5a80fb576c4a2e922d506fe841ee4e |
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| Quellennotiz | uspto-grants-2001_04 |
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