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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 549005생성일: 2026년 10월 24일

4-Toluenesulfonyl chloride → 6-(2-Chloro-5-methoxy-1-methyl-1H-indol-3-yl)-5H-pyrrolo[2,3-b]pyrazine

https://huagongshe.com/ko/reaction/549005

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물6-(5-methoxy-1-methyl-1H-indol-3-yl)-5H-pyrrolo[2,3-b]pyrazineHCID 9860448—
반응물ButyllithiumHCID 178418339—
용매1,1-Dimethoxyethan-1-olHCID 18413361—
생성물6-(2-Chloro-5-methoxy-1-methyl-1H-indol-3-yl)-5H-pyrrolo[2,3-b]pyrazineHCID 983642440%

반응 단계

A solution of 6-(5-methoxy-1-methyl-1H-indol-3-yl)-5H-pyrrolo[2,3-b]pyrazine [100 mg, Example 1(a)] in dimethoxy ethanol (25 mL), cooled to −78° C., was treated with a solution of n-butyllithium in hexanes (172 μl, 2.5M). After stirring for 30 minutes the mixture was treated with 4-toluenesulfonyl chloride (82 mg) then allowed to warm slowly to ambient temperature and then evaporated. The residue was subjected to flash chromatography on silica eluting with a mixture of dichloromethane and methanol (19:1, v/v) to give the title compound (45 mg) as a black solid. MS: 313 (MH+). 1H NMR [(CD3)2SO]: δ 12.20 (1H, s); 8.39 (1H, d, J=3 Hz); 8.21 (1H, d, J=3 Hz); 7.54 (1H, d, J=9 Hz); 7.30 (1H, d, J=2 Hz); 6.96 (1H, dd, J=9 and 2 Hz); 6.84 (1H, d, J=2 Hz); 3.82 (3H, s); 3.81 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07943616B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-f3f6f33e9ced43d58065ad545bf5a068
출처 메모uspto-grants-2011_05