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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70883생성일: 2026년 10월 23일

Sodium Carbonate → (R)-ethyl 3-(tert-butoxycarbonylamino)-4-(2',5'-dichlorobiphenyl-4-yl)butanoate

https://huagongshe.com/ko/reaction/70883

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2,5-Dichlorobenzeneboronic acidHCID 2773371—
반응물(R)-Ethyl 4-(4-bromophenyl)-3-((tert-butoxycarbonyl)amino)butanoateHCID 59607624—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
용매Sodium chloride; waterHCID 57417360—
생성물(R)-ethyl 3-(tert-butoxycarbonylamino)-4-(2',5'-dichlorobiphenyl-4-yl)butanoateHCID 5960766692.7%

반응 조건

온도95 °C

반응 단계

A mixture of (R)-ethyl 4-(4-bromophenyl)-3-(tert-butoxycarbonylamino)butanoate (1.005 g, 2.60 mmol), 2,5-dichlorophenylboronic acid (0.745 g, 3.90 mmol), Pd(PPh3)4 (0.301 g, 0.260 mmol) and 2 M aqueous Na2CO3 (2.60 ml, 5.20 mmol) in 1,2-dimethoxyethane (20 ml) is allowed to stir at 95° C. under nitrogen for 3 hours. The reaction mixture is cooled to room temperature and diluted with brine. The two phases are separated. The products are extracted twice with ethyl acetate (2×100 ml) from the aqueous layer. The combined organic layer is washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The obtained residue is purified by silica gel flash column chromatography (heptane/EtOAc=100:0 to 70:30) to give (R)-ethyl 3-(tert-butoxycarbonylamino)-4-(2′,5′-dichlorobiphenyl-4-yl)butanoate (1.09 g); HPLC retention time=1.50 minutes (condition B); MS (ES+)=352.00 (m-BOC+2; 100%); 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.28 (t, J=7.1 Hz, 3 H) 1.41 (s, 9 H) 2.45-2.58 (m, 2 H) 2.85-3.00 (m, 2 H) 4.17 (t, J=7.1 Hz, 2 H) 4.20 (br s, 1 H) 5.06-5.08 (m, 1 H) 7.23-7.28 (m, 3 H) 7.31-7.40 (m, 4 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822534B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-6096ed87b8c84fda8d76fb191abd16d1
출처 메모uspto-grants-2014_09