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HRID 1578805Erstellt: 26. Oktober 2026

Ethanol → 1,3,5-Trimethyl-6-(2-(2-diethylaminoethoxy)phenyl)-1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one

https://huagongshe.com/reaction/1578805

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
Edukt2-AminophenolHCID 5801—
Edukt1-Chloro-2-(diethylamine)ethane hydrochlorideHCID 13363—
EduktHydrazide (H3N21-)HCID 168365—
EduktSodium ethoxideHCID 2723922—
Edukt1,3-Dimethyl-4-nitro-5-pyrazolecarboxylic acid chlorideHCID 10375624—
EduktPyrazolopyrimidinoneHCID 53630237—
EduktHCID 178514247HCID 178514247—
LösungsmittelAcetic AcidHCID 176—
Produkt1,3,5-Trimethyl-6-(2-(2-diethylaminoethoxy)phenyl)-1H-pyrazolo[4,3-d]pyrimidine-7(6H)-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03939161
Quelldatensatzuspto-grants-1976_02
ORD IDord-3911455a917d407eb578c6f2894bade6
Quellennotizuspto-grants-1976_02