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HRID 40360作成日:2026年10月24日

Trimethyl orthoformate → 5-((5-Fluoropyridin-3-ylamino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione

https://huagongshe.com/ja/reaction/40360

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl orthoformateHCID 9005—
反応物2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
反応物5-Fluoro-3-pyridinamineHCID 574450—
溶媒HexaneHCID 8058—
生成物5-((5-Fluoropyridin-3-ylamino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 6750340782.2%

反応条件

温度100 °C

反応手順

A 150 mL sealed tube was charged with 2,2-dimethyl-1,3-dioxane-4,6-dione (6.0 g, 41.6 mmol) and trimethyl orthoformate (41.6 mL, 41.6 mmol). This was heated to 100° C., and stirred at this temperature for 2 hours. Reaction then cooled to 30° C. and 5-fluoropyridin-3-amine (4.7 g, 41.6 mmol) added portion-wise. Reaction vessel resealed and mixture stirred at 100° C. for 3 hours. LC/MS shows completion. Reaction mixture was cooled to room temperature, diluted with hexane, filtered, and air dried to yield 5-((5-fluoropyridin-3-ylamino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione (9.1 g, 82% yield) as a bright yellow solid. MS [M+H]=267.2. Calc'd for C12H11FN2O4=266.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524900B2
出典データセットuspto-grants-2013_09
ORD IDord-a27c34caba144fe9ae34d3fccb51d828
出典メモuspto-grants-2013_09