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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12974생성일: 2026년 10월 24일

4-Cyanophenylboronic acid → (3aR,6aR)-1-[4'-(2-methoxypyrimidin-5-yl)-1,1'-biphenyl-4-yl]-5-methyloctahydropyrrolo[3,4-b]pyrrole

https://huagongshe.com/ko/reaction/12974

반응식

참여 물질

역할이름HCID투입량
반응물4-Cyanophenylboronic acidHCID 2734326—
반응물2-Methoxypyrimidine-5-boronic acidHCID 2736778—
반응물(3aR,6aR)-1-(4-Bromophenyl)-5-methyloctahydropyrrolo[3,4-b]pyrroleHCID 44221503—
생성물(3aR,6aR)-1-[4'-(2-methoxypyrimidin-5-yl)-1,1'-biphenyl-4-yl]-5-methyloctahydropyrrolo[3,4-b]pyrroleHCID 24743816—

반응 단계

The title compound was prepared according to the procedure described in Example 7D, substituting the product of Example 41A for the product of Example 7C and substituting 2-methoxy-pyrimidine-5-boronic acid for 4-cyanophenylboronic acid. 1H NMR (500 MHz, CDCl3) δ ppm 8.76 (s, 2H) 7.66 (d, J=8.54 Hz, 2H) 7.53 (dd, J=11.75, 8.70 Hz, 4H) 6.67 (d, J=8.85 Hz, 2H) 4.13-4.22 (m, 1H) 4.07 (s, 3H) 3.53-3.61 (m, 1H) 3.26-3.35 (m, 1H) 2.91-3.03 (m, 1H) 2.71-2.77 (m, 1H) 2.48-2.67 (m, 3H) 2.33 (s, 3H) 2.13-2.25 (m, 1H) 1.90-2.01(m, 1H). MS, (M+H)+=387.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728031B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7ec783b5cf594ccfb60f56e13e3479b9
출처 메모uspto-grants-2010_06