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HRID 2079898作成日:2026年10月27日

Potassium Hydroxide → 4-(1-cyclopentyl-6-nitro-1H-indol-3-yl)-benzonitrile

https://huagongshe.com/reaction/2079898

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物Cyclopentyl 4-methylbenzene-1-sulfonateHCID 317685—
反応物4-(6-nitro-1H-indol-3-yl)-benzonitrileHCID 57442197—
溶媒Dimethyl SulfoxideHCID 679—
生成物4-(1-cyclopentyl-6-nitro-1H-indol-3-yl)-benzonitrileHCID 5744224458%

反応手順

Method M Add KOH pellets (200 mg, 3.42 mmol) to a solution of 4-(6-nitro-1H-indol-3-yl)-benzonitrile, 9, (150 mg, 0.57 mmol) in DMSO (10 mL). After the KOH pellets dissolve, add cyclopenyl tosylate (210 mg, 0.85 mmol) in DMSO (3 mL). Allow the reaction mixture to stir overnight at ambient temperature. Add additional cyclopentyl tosylate (210 mg, 0.85) and allow the reaction mixture to stir for another 6 h. Add still more cyclopentyl tosylate (210 mg, 0.85 mmol) and allow the reaction mixture to stir overnight at ambient temperature. Quench the resulting reaction mixture with 5N HCl/ice. Extract the quenched reaction mixture with EtOAc. Wash the EtOAc extracts with brine. Dry the organic layer over MgSO4, filter, and remove the solvent from the filtrate to provide a solid. Purify by silica gel column chromatography (0-100% EtOAc/hexanes gradient) and collect the fractions and remove the solvent to afford 110 mg (58%) of the title compound. LRMS (API ES+)=332.2 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07932284B2
出典データセットuspto-grants-2011_04
ORD IDord-59925e9d0a3643939c0cd70ec81fdb67
出典メモuspto-grants-2011_04