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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84794생성일: 2026년 10월 25일

Hydrogen Peroxide → 4-((1R,2S)-2-aminocyclohexylamino)-2-(1-methyl-1H-indol-4-ylamino)benzamide

https://huagongshe.com/reaction/84794

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물tert-butyl (1S,2R)-2-(4-cyano-3-(1-methyl-1H-indol-4-ylamino)phenylamino)cyclohexylcarbamateHCID 69283979—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물4-((1R,2S)-2-aminocyclohexylamino)-2-(1-methyl-1H-indol-4-ylamino)benzamideHCID 5733402613.9%

반응 단계

To a solution of tert-butyl (1S,2R)-2-(4-cyano-3-(1-methyl-1H-indol-4-ylamino)phenylamino)cyclohexylcarbamate (90 mg, 0.19 mmol) in DMSO (2 mL). K2CO3 (130 mg, 0.94 mmol) and H2O2 (50% aq., 0.500 mL) were added. The mixture was stirred at 100 C for 10 min. Water and EtOAc were added. The organic phase was separated, dried over Na2SO4, concentrated in vacuo. The residue was dissolved in TFA (2 mL). After 10 min of standing, TFA was removed in vacuo. The residue was purified by HPLC to give the titled compound (10 mg). MS 378.3 (M+H); UV 224.7, 291.5 nm

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846928B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-cb73c02deddc499bb962f4b456490400
출처 메모uspto-grants-2014_09