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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572503생성일: 2026년 10월 26일

Methyl [7-bromo-4-(3,4-dimethylphenyl)-2-methyl-1-oxo-1,2-dihydro-3-isoquinolinyl][(1,1-dimethylethyl)oxy]acetate → 2-Tert-butoxy-2-[4-(3,4-dimethylphenyl)-7-isobutyl-2-methyl-1-oxo-3-isoquinolyl]acetic acid

https://huagongshe.com/reaction/572503

반응식

참여 물질

역할이름HCID투입량
반응물Methyl [7-bromo-4-(3,4-dimethylphenyl)-2-methyl-1-oxo-1,2-dihydro-3-isoquinolinyl][(1,1-dimethylethyl)oxy]acetateHCID 68295047—
반응물HCID 178448254HCID 178448254—
생성물2-Tert-butoxy-2-[4-(3,4-dimethylphenyl)-7-isobutyl-2-methyl-1-oxo-3-isoquinolyl]acetic acidHCID 71596144—

반응 단계

The title compound was prepared in two steps in a manner similar to that described in Example 171 from methyl 2-(7-bromo-4-(3,4-dimethylphenyl)-2-methyl-1-oxo-1,2-dihydroisoquinolin-3-yl)-2-(tert-butoxy)acetate and isobutylzinc(II) bromide and was isolated as a white solid (11.7 mg, 37%) after reverse phase chromatography: 1H NMR (400 MHz, CHLOROFORM-d) δ=8.27 (s, 1 H), 7.42-7.22 (m, 3 H), 7.16-7.00 (m, 2 H), 5.35 (m, 1 H), 3.70 (s, 3 H), 2.61 (m, 2 H), 2.36 (m, 3 H), 2.32 (m, 3 H), 2.00-1.85 (m, 1 H), 1.07 (m, 9 H), 0.96-0.85 (m, 6 H); LC/MS (m/z) ES+=450 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029391B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-14d7f769988743179b6999bbe4e40a94
출처 메모uspto-grants-2015_05