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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84793생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/84793

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 번호US08846928B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-dee26ad7db884a5ea672e23ab9821c8a
출처 메모uspto-grants-2014_09