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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383604생성일: 2026년 10월 23일

Nitrogen → {2'-[3-(3,4,5-Trihydroxy-phenyl)-propionylamino]-biphenyl-3-yl}-acetic acid methyl ester

https://huagongshe.com/ko/reaction/383604

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Boron tribromideHCID 25134—
반응물{2'-[3-(3,4,5-Trimethoxy-phenyl)-propionylamino]-biphenyl-3-yl}-acetic acid methyl esterHCID 16116560—
용매DichloromethaneHCID 6344—
생성물{2'-[3-(3,4,5-Trihydroxy-phenyl)-propionylamino]-biphenyl-3-yl}-acetic acid methyl esterHCID 598198465%

반응 조건

온도-78 °C

반응 단계

(The following reaction is done in an anhydrous N2 atmosphere.) Dissolve {2′-[3-(3,4,5-Trimethoxy-phenyl)-propionylamino]-biphenyl-3-yl}-acetic acid methyl ester (72) (46 mg, 0.10 mmol) in anhydrous DCM (1.0 mL), cool the solution to −78° C. and add dropwise BBr3 (85 μL, 0.90 mmol). Stir the reaction mixture for 30 min at −78° C. and after slowly warming up for additional 2 h at rt. Add dropwise ice water, separate layers and extract aqu. layer with DCM (3 times). Wash combined organic layer with brine and dry with Na2SO4. Purify the crude product by preparative RP HPLC (gradient, water/CH3CN 95:5 to 5:95) to obtain {2′-[3-(3,4,5-Trihydroxy-phenyl)-propionylamino]-biphenyl-3-yl}-acetic acid methyl ester (73) (2 mg, 5%). 1H NMR (400 MHz, CD3CN): 2.43 (t, 2H, J=7.6 Hz); 2.69 (t, 2H, J=7.6 Hz); 3.66 (s, 3H); 3.70 (s, 2H); 6.25 (s, 2H); 7.18-7.34 (m, 5 H); 7.35-7.44 (m, 2H); 7.65 (br.s, 1H); 7.89 (br.d, 1H, J=8.3 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367677B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-a9dcd5bfeff7454cb3cd57ea2b25269b
출처 메모uspto-grants-2013_02