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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24631생성일: 2026년 10월 26일

Potassium Carbonate → N-(2,6-Dichlorobenzoyl)-4-[2-[N-(tert-butyl)sulfamoyl]phenyl]-L-phenylalanine methyl ester

https://huagongshe.com/reaction/24631

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Boronic acid, B-(2-(((1,1-dimethylethyl)amino)sulfonyl)phenyl)-HCID 4997616—
반응물N-(2,6-dichlorobenzoyl)-4-bromo-L-phenylalanine methyl esterHCID 54284267—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
용매Ethyl AcetateHCID 8857—
생성물N-(2,6-Dichlorobenzoyl)-4-[2-[N-(tert-butyl)sulfamoyl]phenyl]-L-phenylalanine methyl esterHCID 5390675876.5%

반응 조건

온도80 °C

반응 단계

2-[N-(tert-Butyl)sulfamoyl]benzeneboronic acid (0.4 g) was dissolved in DME (10 mL). To this solution was added K2CO3 (0.1 g), N-(2,6-dichlorobenzoyl)-4-bromo-L-phenylalanine methyl ester (0.1 g), Pd(Ph3P)4 (0.1 g) and water (0.2 mL). The mixture was heated at 80° C. overnight. After cooling, EtOAc and water were added to the mixture. The EtOAc phase was dried (MgSO4), filtered and evaporated. The residue was purified by flash column chromatography (silica gel; eluent: EtOAc/hexanes 1:2) to give 100 mg of the title compound. ESMS: m/z 585 ([M+Na]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855843B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-3fbb1750900f439ba20a4652ef70f839
출처 메모uspto-grants-2005_02