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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 반응물 | 6-(5-methoxy-1-methyl-1H-indol-3-yl)-5H-pyrrolo[2,3-b]pyrazine | HCID 9860448 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | 1,1-Dimethoxyethan-1-ol | HCID 18413361 | — |
| 생성물 | 6-(2-Chloro-5-methoxy-1-methyl-1H-indol-3-yl)-5H-pyrrolo[2,3-b]pyrazine | HCID 9836424 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07943616B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-f3f6f33e9ced43d58065ad545bf5a068 |
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| 출처 메모 | uspto-grants-2011_05 |
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