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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 593501생성일: 2026년 10월 24일

4-(Methylsulfonyl)benzyl Bromide → 1-(4-methanesulfonyl-benzyl)-3-methyl-2-pyridin-3-yl-1H-indole

https://huagongshe.com/ko/reaction/593501

반응식

참여 물질

역할이름HCID투입량
반응물4-(Methylsulfonyl)benzyl BromideHCID 2733581—
반응물3-Methyl-2-(3-pyridyl)indole hydrochlorideHCID 44553961—
생성물1-(4-methanesulfonyl-benzyl)-3-methyl-2-pyridin-3-yl-1H-indoleHCID 44554309—

반응 단계

3-Methyl-2-pyridin-3-yl-1H-indole hydrochloride (Example 1) and 1-bromomethyl-4-methanesulfonyl-benzene are processed according to the method described in Example 11 to give 1-(4-methanesulfonyl-benzyl)-3-methyl-2-pyridin-3-yl-1H-indole. 1H NMR (400 MHz, MeOD) δ ppm 2.33 (s, 3H), 3.08 (s, 3H), 5.46 (s, 2H), 7.08 (d, J=8.1 Hz, 2H), 7.18 (t, J=7.3 Hz, 1H), 7.24 (t, J=7.6 Hz, 1H), 7.34 (d, J=8.1 Hz, 1H), 7.55 (dd, J=7.8, 4.8 Hz, 1H), 7.68 (d, J=7.8 Hz, 1H), 7.81 (d, J=8.3 Hz, 2H), 7.85 (dt, J=7.8, 1.9 Hz, 1H), 8.52 (d, J=2.3 Hz, 1H), 8.59 (dd, J=4.9, 1.6 Hz, 1H). HRMS (ESI) m/z 377.1318 [(M+H)+ Calcd for C22H21N2O2S: 377.1324].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242963B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-6323549059e34d589bed6c294caa19ee
출처 메모uspto-grants-2016_01