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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70314생성일: 2026년 10월 24일

Dichloromethane → 1,1-Dimethylethyl (2-{[3'-(aminocarbonyl)-2-methyl-4-biphenylyl]oxy}ethyl)carbamate

https://huagongshe.com/ko/reaction/70314

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Sodium CarbonateHCID 10340—
반응물(3-Carbamoylphenyl)boronic acidHCID 2737814—
반응물1,1-Dimethylethyl {2-[(4-bromo-3-methylphenyl)oxy]ethyl}carbamateHCID 59316461—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매1,2-DimethoxyethaneHCID 8071—
생성물1,1-Dimethylethyl (2-{[3'-(aminocarbonyl)-2-methyl-4-biphenylyl]oxy}ethyl)carbamateHCID 59316381—

반응 조건

온도80 °C

반응 단계

A mixture of 1,1-dimethylethyl {2-[(4-bromo-3-methylphenyl)oxy]ethyl}carbamate (0.102 g, 0.31 mmol; Example V-15), 3-(aminocarbonyl)phenylboronic acid (0.056 g; 0.34 mmol), PdCl2(dppf).CH2Cl2 (0.0075 g; 0.01 mmol), DME (2 mL) and 2M Na2CO3 (2 mL) was degassed by sparging with N2,(5-10 min) then stirred at 80° C. for 5.5 h. Upon cooling, the mixture was diluted with EtOAc washed (water, brine), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography (EtOAc/hexanes), affording the title compound as a colorless foam. LC/MS (method A) 2.59 min, m/z 371 (M+1, 2%), 392 (M+Na, 53%), 271 ([M−Boc]+H, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822518B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-48addb1084d54c4889c0e9cb3eea88f2
출처 메모uspto-grants-2014_09