HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethanol → 1,3,5-Trimethyl-6-(2-(2-diethylaminoethoxy)phenyl)-1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | 2-Aminophenol | HCID 5801 | — |
| Edukt | 1-Chloro-2-(diethylamine)ethane hydrochloride | HCID 13363 | — |
| Edukt | Hydrazide (H3N21-) | HCID 168365 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | 1,3-Dimethyl-4-nitro-5-pyrazolecarboxylic acid chloride | HCID 10375624 | — |
| Edukt | Pyrazolopyrimidinone | HCID 53630237 | — |
| Edukt | HCID 178514247 | HCID 178514247 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 1,3,5-Trimethyl-6-(2-(2-diethylaminoethoxy)phenyl)-1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one | HCID 21558538 | — |
Reaktionsschritte
1,3-Dimethyl-4-nitro-5-pyrazolecarboxylic acid chloride is reacted with an equimolar quantity of o-aminophenol and the resulting nitroamide is catalytically reduced to the amino amide. Following the method of Example 2, the amino amide is cyclized with acetic acid in an autoclave and the resulting pyrazolopyrimidone is treated with an equimolar amount of diethylaminoethylchloride hydrochloride in absolute ethanol containing two equivalents of sodium ethoxide. 1,3,5-Trimethyl-6-(2-(2-diethylaminoethoxy)phenyl)-1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one is obtained from the reaction mixture.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US03939161 |
| Quelldatensatz | uspto-grants-1976_02 |
| ORD ID | ord-3911455a917d407eb578c6f2894bade6 |
| Quellennotiz | uspto-grants-1976_02 |