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HRID 397008作成日:2026年10月25日

Ethyl bromoacetate → Ethyl 3,6-dihydro-3-(methoxymethyl)-5-nitro-2,6-dioxo-1(2H)-pyrimidineacetate

https://huagongshe.com/reaction/397008

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物5-Nitro-1-methoxymethyluracilHCID 18172488—
溶媒TetrahydrofuranHCID 8028—
溶媒Tetrabutylammonium FluorideHCID 2724141—
生成物Ethyl 3,6-dihydro-3-(methoxymethyl)-5-nitro-2,6-dioxo-1(2H)-pyrimidineacetateHCID 21355699—

反応手順

The compound of example 41 (10.0 g, 50 mmole) is dissolved in tetrabutylammonium flouride (120 mL of a 1.0M solution in tetrahydrofuran, 0.124 mole). Ethyl bromoacetate (8.3 mL, 75 mmole) is added. The reaction is stirred at room temperature. The reaction mixture is concentrated, then partitioned between dichloromethane and water. The aqueous layer is extracted with dichloromethane. The combined organic extracts are washed with water, brine, and dried over anhydrous magnesium sulfate. The solvent is removed under vacuum to afford the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06608204B1
出典データセットuspto-grants-2003_08
ORD IDord-96a36b6cadd045c68beeb6ee26e579cb
出典メモuspto-grants-2003_08