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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84797생성일: 2026년 10월 23일

Potassium Carbonate → tert-butyl (1S,2R)-2-(3-(3-(2H-1,2,3-triazol-2-yl)phenylamino)-4-cyanophenylamino)cyclohexylcarbamate

https://huagongshe.com/ko/reaction/84797

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Binap, (A+-)-HCID 634876—
반응물3-(2H-1,2,3-Triazol-2-yl)anilineHCID 23438756—
반응물tert-butyl (1S,2R)-2-(3-bromo-4-cyanophenylamino)cyclohexylcarbamateHCID 69283621—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl (1S,2R)-2-(3-(3-(2H-1,2,3-triazol-2-yl)phenylamino)-4-cyanophenylamino)cyclohexylcarbamateHCID 69284027—

반응 단계

A mixture of tert-butyl (1S,2R)-2-(3-bromo-4-cyanophenylamino)cyclohexylcarbamate (150 mg, 0.380 mmol), 3-(2H-1,2,3-triazol-2-yl)aniline (100 mg, 0.625 mmol), BINAP (40 mg, 0.064 mmol), Pd(OAc)2 (25 mg, 0.11 mmol) and K2CO3 (150 mg, 1.08 mmol) in dioxane (3 mL) was degassed with Ar, then was stirred at 100 C for 4 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 to give tert-butyl (1S,2R)-2-(3-(3-(2H-1,2,3-triazol-2-yl)phenylamino)-4-cyanophenylamino)cyclohexylcarbamate as a crude residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846928B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3880bfdab573446e805326443415ea25
출처 메모uspto-grants-2014_09