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HRID 132859作成日:2026年10月26日

Formamidine acetate → tert-Butyl 7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate

https://huagongshe.com/reaction/132859

反応式

関与物質

役割名称HCID仕込み量
反応物Formamidine acetateHCID 160693—
反応物Sodium ethoxideHCID 2723922—
反応物tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylateHCID 53395404—
溶媒EthanolHCID 702—
生成物tert-Butyl 7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylateHCID 22707088—

反応手順

Formamidine acetate (472 mg, 4.52 mmol) in 15.0 mL of absolute ethanol was treated with sodium ethoxide (21 wt % solution in ethanol; 1.7 mL). After 30 min, a solution of the product from Step A above (1.15 g) in 8 mL of absolute ethanol was added, and the mixture was warmed at reflux for 18 h. The dark solution was cooled to room temperature and concentrated under reduced pressure, and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with brine, dried over magnesium sulfate and concentrated to an orange oil. Purification by flash chromatography (silica gel; 2% methanol/dichloromethane as eluant) afforded the title compound as a light yellow gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07388019B2
出典データセットuspto-grants-2008_06
ORD IDord-66ae1acf66014a01b5eaced42a3466dd
出典メモuspto-grants-2008_06