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HRID 238503作成日:2026年10月26日

6-Nitroindoline → 1-(1-Methyl(4-piperidyl))-6-nitroindoline

https://huagongshe.com/reaction/238503

反応式

関与物質

役割名称HCID仕込み量
反応物6-NitroindolineHCID 29757—
反応物1-Methyl-4-piperidoneHCID 74049—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒Acetic AcidHCID 176—
溶媒1,1-DichloroethaneHCID 6365—
生成物1-(1-Methyl(4-piperidyl))-6-nitroindolineHCID 18796623—

反応手順

6-Nitroindoline (5 g) was dissolved in 200 mL of dichloroethane, N-methyl-4-piperidone (5 g) was added to the mixture, followed by 12 g NaBH(OAc)3 and 1 mL of glacial AcOH. The mixture was stirred at RT overnight. Saturated NaHCO3 solution (200 mL) was added to the reaction mixture and stirred for 1 h. The resulting mixture was separated by separation funnel, the organic layer was extracted once with saturated NaHCO3 solution and once with brine. The resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel with 2:1 EtOAc:MeOH to afford an orange oil. MS: 262 (M+1). Calc'd. for C14H19N3O2—261.32.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642624B2
出典データセットuspto-grants-2014_02
ORD IDord-7d1fd85e774f4ec59f2291df1b4171fd
出典メモuspto-grants-2014_02