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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1677400생성일: 2026년 10월 27일

4-Toluenesulfonyl chloride → 7-iodo-5-(toluene-4-sulfonyl)-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine

https://huagongshe.com/reaction/1677400

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Sodium hydrideHCID 24758—
반응물7-iodo-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazineHCID 59540518—
용매TetrahydrofuranHCID 8028—
생성물7-iodo-5-(toluene-4-sulfonyl)-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazineHCID 5954074494.3%

반응 조건

온도0 °C

반응 단계

7-Iodo-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine (371 mg, 0.9 mmol) was suspended in 5 ml of THF and cooled to 0° C. in an ice bath. Sodium hydride, 60% dispersion in mineral oil (43 mg, 1.08 mmol) was added and the suspension was stirred for 20 minutes. 4-Methyl-benzenesulfonyl chloride (189 mg, 0.99 mmol) was added, the ice bath was removed, and the reaction was stirred at room temperature for 3 hours. The solvent was evaporated on a rotary evaporator. The residue was triturated with 1M potassium hydroxide. The solid was filtered, washed with water, and dried to yield 480 mg of 7-iodo-5-(toluene-4-sulfonyl)-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008298B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-7e90248477c94ec6b75bddd8661369fe
출처 메모uspto-grants-2011_08