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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2201024생성일: 2026년 10월 24일

Potassium Carbonate → tert-butyl (1S,2R)-2-(4-cyano-3-(1-methyl-1H-indol-4-ylamino)phenylamino)cyclohexylcarbamate

https://huagongshe.com/ko/reaction/2201024

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Binap, (A+-)-HCID 634876—
반응물1-methyl-1H-indol-4-amineHCID 22170307—
반응물tert-butyl (1S,2R)-2-(3-bromo-4-cyanophenylamino)cyclohexylcarbamateHCID 69283621—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl (1S,2R)-2-(4-cyano-3-(1-methyl-1H-indol-4-ylamino)phenylamino)cyclohexylcarbamateHCID 6928397939.5%

반응 단계

A mixture of tert-butyl (1S,2R)-2-(3-bromo-4-cyanophenylamino)cyclohexylcarbamate (200 mg, 0.507 mmol), 1-methyl-1H-indol-4-amine (160 mg, 1.09 mmol), BINAP (50 mg, 0.080 mmol), Pd(OAc)2 (25 mg, 0.11 mmol) and K2CO3 (150 mg, 1.08 mmol) in dioxane (4 mL) was degassed with Ar, then was stirred at 100 C for 16 h. EtOAc and water were added. The organic phase was separated, washed with 1N HCl, then with 5% NaHCO3, dried over Na2SO4, concentrated in vacuo. The residue was purified by a silica gel column, eluted with 10-40% EtOAc in hexane to give tert-butyl (1S,2R)-2-(4-cyano-3-(1-methyl-1H-indol-4-ylamino)phenylamino)cyclohexylcarbamate (92 mg) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09359375B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-dd14cd62c92b42cebd69d74246b9436c
출처 메모uspto-grants-2016_06