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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2079898생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2079898

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Cyclopentyl 4-methylbenzene-1-sulfonateHCID 317685—
반응물4-(6-nitro-1H-indol-3-yl)-benzonitrileHCID 57442197—
용매Dimethyl SulfoxideHCID 679—
생성물4-(1-cyclopentyl-6-nitro-1H-indol-3-yl)-benzonitrileHCID 5744224458%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07932284B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-59925e9d0a3643939c0cd70ec81fdb67
출처 메모uspto-grants-2011_04