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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63956생성일: 2026년 10월 26일

2-(2-Fluoro-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → (2S)-2-tert-butoxy-2-[4-(2-fluoro-4-methyl-phenyl)-2-methyl-5,6,7,8-tetrahydrobenzothiopheno[2,3-b]pyridin-3-yl]acetic acid

https://huagongshe.com/reaction/63956

반응식

참여 물질

역할이름HCID투입량
반응물2-(2-Fluoro-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 69672435—
반응물Methyl (2S)-tert-butoxy(4-iodo-2-methyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridin-3-yl)acetateHCID 69673123—
생성물(2S)-2-tert-butoxy-2-[4-(2-fluoro-4-methyl-phenyl)-2-methyl-5,6,7,8-tetrahydrobenzothiopheno[2,3-b]pyridin-3-yl]acetic acidHCID 67606987—

반응 단계

The title compound was prepared from Methyl (2S)-tert-butoxy(4-iodo-2-methyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridin-3-yl)acetate (Preparation 16, 100 mg, 212 μmol) and 2-(2-fluoro-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (Preparation 19, 99 mg, 424 μmol) using the same method as described in Example 44, Step 1 to yield 100 mg, 96%. Material obtained was a mixture of atropisomers, in a 2:1 ratio.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447116B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-152c528b701e4d7d915168ee7514cdba
출처 메모uspto-grants-2016_09