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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273525생성일: 2026년 10월 26일

Sodium Carbonate → N-[3-(3-amino-5-methyl-benzo[1,2,4]triazin-7-yl)-phenyl]-methanesulfonamide

https://huagongshe.com/reaction/273525

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물3-Methylsulfonylaminophenylboronic acidHCID 2773535—
반응물7-Bromo-5-methylbenzo[e][1,2,4]triazin-3-amineHCID 24822752—
촉매HCID 178418397HCID 178418397—
생성물N-[3-(3-amino-5-methyl-benzo[1,2,4]triazin-7-yl)-phenyl]-methanesulfonamideHCID 5983762482%

반응 단계

An oven dried 25 mL round bottom flask was charged with 7-bromo-5-methyl-benzo[1,2,4]triazin-3-ylamine (0.889 g, 3.72 mmol, 1 equiv), 3-(methylsulfonylamino) phenyl boronic acid (1.12 g, 5.21 mmol, 1.4 equiv), sodium carbonate (1.57 g, 14.9 mmol, 4 equiv) and tetrakis(triphenylphosphine)palladium(0) (0.43 g, 0.372 mmol, 0.1 equiv). The reactants were flushed with argon and diluted with ethylene glycol dimethyl ether (20 mL), ethanol (5 mL) and DI water (5 mL). The reaction vessel was outfitted with condenser and refluxed for 4 hours. The reaction was filtered hot and diluted with ethyl acetate. The Organic layer was isolated and concentrated to a dark residue. This was dissolved in DMF (6 mL) and slowly diluted with water so as to precipitate out the product. Solids were filtered off and dried to yield an orange solid (1 g, 82% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456176B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-9a1edb7d233d4b0f909c2c1d1738825f
출처 메모uspto-grants-2008_11