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HRID 41574作成日:2026年10月24日

3-Bromoquinoline → 9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one

https://huagongshe.com/ja/reaction/41574

反応式

関与物質

役割名称HCID仕込み量
反応物3-BromoquinolineHCID 21413—
反応物2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
反応物Sodium t-butoxideHCID 23676156—
反応物2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-oneHCID 67251512—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒1,4-DioxaneHCID 31275—
生成物9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-oneHCID 6725113772.6%

反応条件

温度100 °C

反応手順

The mixture of 2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one (100 mg, 0.15 mmol, contains 1.7 moleq TFA), 3-bromoquinoline (49 mg, 0.23 mmol), Pd2dba3 (7 mg, 7.7 μmol), sodium t-butanolate (45 mg, 0.46 mmol), 2-(2-dicyclohexylphosphanylphenyl)-N,N-dimethylaniline (DavePhos, 6.1 mg, 0.015 mmol) and dry dioxane (2 mL) was placed in a microwave tube and flushed with argon. The tube was sealed and the suspension was heated at 100° C. for 1 h under microwave conditions. The reaction mixture was diluted with ethyl acetate and washed with water and brine and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting brown oil was purified by flash chromatography (EtOAc/heptane 3:1) to yield the title compound (63 mg, 68%). [LCMS RtA=1.31 min, [M+H]+=579.2].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530648B2
出典データセットuspto-grants-2013_09
ORD IDord-54e8e8e4441743bbb73db5a0c3ee97d0
出典メモuspto-grants-2013_09