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HRID 216759作成日:2026年10月26日

Dabco → HCID 178424198、化合物

https://huagongshe.com/reaction/216759

反応式

関与物質

役割名称HCID仕込み量
反応物DabcoHCID 9237—
反応物Sodium hydrideHCID 24758—
反応物6-ChloropurineHCID 5359277—
反応物(8-Methyl-2-o-tolylquinolin-3-yl)methanolHCID 57707986—
溶媒Acetic AcidHCID 176—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Sodium chloride; waterHCID 57417360—
生成物HCID 178424198HCID 178424198—

反応手順

Prepared according to procedure L A mixture of 6-chloropurine (110 mg, 0.71 mmol) and 1,4-diazabicyclo[2.2.2]octane (160 mg, 1.43 mmol) in DMSO (0.7 mL) was stirred at rt for 4 h and was then added via cannula to a mixture of (8-methyl-2-o-tolylquinolin-3-yl)methanol (94 mg, 0.36 mmol) and sodium hydride, 60% dispersion in mineral oil (57 mg, 1.43 mmol) in DMSO (1 mL) that had been stirred at rt for 15 min prior to the addition. The mixture was stirred at rt for 3.5 h, neutralized by the addition of glacial acetic acid, diluted with brine (15 mL), and extracted with EtOAc (3×15 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure. The resulting yellow oil was dissolved in CH2Cl2, evaporated onto silica gel (deactivated with 2M NH3 in MeOH), and purified by flash chromatography (Biotage® Si 25+M) eluting with 2 M NH3 in MeOH/CH2Cl2 (5%) to provide a white solid [PI3δ IC50=27 nM]. MS (APCI+) m/z=282.3 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193199B2
出典データセットuspto-grants-2012_06
ORD IDord-76503cf13c79468a84ad45caee737755
出典メモuspto-grants-2012_06