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HRID 334132作成日:2026年10月25日

N,N,N',N'-Tetramethylethylenediamine → HCID 86667350、化合物

https://huagongshe.com/reaction/334132

反応式

関与物質

役割名称HCID仕込み量
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物HexaneHCID 8058—
反応物1-Chloro-2-iodoethaneHCID 136438—
反応物HCID 86667351HCID 86667351—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 86667350HCID 8666735078.5%

反応条件

温度0 °C

反応手順

A solution of 4-(2-chloro-6-morpholino-9H-purin-9-yl)-2-methylbutan-2-ol (360 mg, 1.1 mmol) and N,N,N′,N′-tetramethylethylenediamine (0.25 mL, 1.7 mmol) in THF (8.1 mL) was cooled to −42° C. and treated with a solution of 2.5M n-butyllithium in hexane (BuLi, 2.0 mL, 5.0 mmol) dropwise over 5 minutes. After 30 minutes at −42° C., 1-chloro-2-iodoethane (0.51 mL, 5.4 mmol) was added and the reaction mixture was slowly warmed to 0° C. over 1 hr. The mixture was quenched with a saturated solution of NH4Cl, and diluted with ethyl acetate. The aqueous layer was extracted into ethyl acetate (3×), and the combined organics were dried over sodium sulfate, filtered, and absorbed onto celite for purification by flash chromatography to afford 4-(2-chloro-8-iodo-6-morpholino-9H-purin-9-yl)-2-methylbutan-2-ol as a white foam (390 mg, 78%). LC/MS (ESI+): m/z 452 (M+H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883799B2
出典データセットuspto-grants-2014_11
ORD IDord-3abe81a3204e4a34be21a45b4d36d231
出典メモuspto-grants-2014_11