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HRID 1692874作成日:2026年10月25日

Sodium triacetoxyborohydride → 2-(1-((2-chloro-6-morpholino-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-8-yl)methyl)piperidin-4-yl)propan-2-ol

https://huagongshe.com/reaction/1692874

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物2-(4-Piperidyl)-2-propanolHCID 5200321—
反応物2-chloro-6-morpholin-4-yl-9-(tetrahydropyran-2-yl)-9H-purine-8-carbaldehydeHCID 59603464—
溶媒1,2-DichloroethaneHCID 11—
溶媒Sodium BicarbonateHCID 516892—
生成物2-(1-((2-chloro-6-morpholino-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-8-yl)methyl)piperidin-4-yl)propan-2-olHCID 5960353998.4%

反応手順

A mixture of 2-chloro-6-morpholino-9-(tetrahydro-2H-pyran-2-yl)-9H-purine-8-carbaldehyde (245 mg, 0.696 mmol), 2-(4-piperidyl)-2-propanol (110 mg, 0.77 mmol) and sodium triacetoxyborohydride (162 mg, 0.77 mmol) in 1,2-dichloroethane (10 mL) was stirred at room temperature for 30 minutes. The reaction mixture was then diluted with saturated aqueous sodium bicarbonate. The aqueous layer was then extracted with DCM. The combined organic extracts were then washed with water, dried over sodium sulfate, filtered and concentrated. The crude product was purified by flash chromatography (0-100% gradient EtOAc-heptane) to give the title compound (328 mg, 98%). LCMS: M+H+=480.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08158625B2
出典データセットuspto-grants-2012_04
ORD IDord-2e57d51323a34bf2ab721a3ded651eae
出典メモuspto-grants-2012_04