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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1677402생성일: 2026년 10월 25일

Acetone → 1-phenyl-2-[5-(toluene-4-sulfonyl)-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-ethanone

https://huagongshe.com/reaction/1677402

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Sulfuric AcidHCID 1118—
반응물7-phenylethynyl-5-(toluene-4-sulfonyl)-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazineHCID 59540633—
촉매Mercuric sulfateHCID 24544—
용매WaterHCID 962—
생성물1-phenyl-2-[5-(toluene-4-sulfonyl)-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-ethanoneHCID 5954100661.8%

반응 조건

온도110 °C

반응 단계

7-Phenylethynyl-5-(toluene-4-sulfonyl)-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine (154 mg, 0.29 mmol), mercury(II) sulfate (127 mg, 0.43 mmol), concentrated sulfuric acid (0.031 ml, 0.58 mmol) and 3 ml of a 3:1 mixture of acetone and water were added to a 5 ml microwave vial. The reaction was heated in a microwave reactor at 110° C. for one hour. The solvent was evaporated and ethyl acetate and aqueous sodium carbonate were added to the residue. The aqueous layer was removed using a reparatory funnel, the organic layer was washed with water twice, then dried and concentrated. The residue was purified by flash chromatography using a gradient of 0% ethyl acetate in hexanes up to 30% to give 100 mg of 1-phenyl-2-[5-(toluene-4-sulfonyl)-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-ethanone as the major product. MS: (M+H)+=558.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08008298B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-e3c1f3e308244fa99f00fc54b8056399
출처 메모uspto-grants-2011_08