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HRID 1738802作成日:2026年10月25日

Propentofylline → HCID 21839364、化合物

https://huagongshe.com/reaction/1738802

反応式

関与物質

役割名称HCID仕込み量
反応物PropentofyllineHCID 4938—
反応物Silanamine, 1,1,1-trimethyl-N-2-propynyl-N-(trimethylsilyl)-HCID 10932630—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物HCID 21839364HCID 21839364—

反応手順

29 ml (46.5 mmol) of a 15% strength butyllithium solution in n-hexane were slowly added dropwise to a stirred solution of 9.26 g (46.5 mmol) of N,N-bis(trimethylsilyl)-2-propynylamine from stage C1 in 50 ml of tetrahydrofuran at -40° C. under argon. The mixture was then warmed to room temperature and again cooled to -40° C., and a solution of 14.25 g (46.5 mmol) of 3-methyl-1-(5-oxohexyl)-7-propylxanthine in 40 ml of tetrahydrofuran was slowly added. After removal of the cooling bath, the mixture was stirred at room temperature for 6 hours. The reaction mixture was then added to saturated ammonium chloride solution at 0° C., the aqueous phase was extracted with ether, the organic phase was dried over sodium sulfate, the desiccant was filtered off, and the solvent was removed under reduced pressure. The crude product was subjected to flash chromatography first with the mobile phase mixture dichloromethane/methanol/saturated ammonia solution=19/1.5/2.5 and then with 9/1/2.5. Yield: 9.79 g (58% of theory); yellowish oil

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05965555
出典データセットuspto-grants-1999_10
ORD IDord-0232de4cd7c1403cb294567411c480f6
出典メモuspto-grants-1999_10