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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 449224생성일: 2026년 10월 25일

Cesium carbonate → 4-[5-methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-yl amino]-N-(2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide

https://huagongshe.com/reaction/449224

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물4-Bromo-N-(2-(pyrrolidin-1-yl)ethyl)benzenesulfonamideHCID 4033090—
반응물5-Methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-ylamineHCID 59837607—
촉매Tris(dibenzylideneacetone) dipalladiumHCID 9832798—
생성물4-[5-methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-yl amino]-N-(2-pyrrolidin-1-yl-ethyl)-benzenesulfonamideHCID 5983768439%

반응 단계

In a dry 25 mL round bottom flask, 5-methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-ylamine (0.223 g, 0.7935 mmol, 1 equiv), 4-bromo-N-(2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide (0.396 g, 1.19 mmol, 1.5 equiv), cesium carbonate (0.776 g, 2.38 mmol, 3 equiv), 4,5-bis(diphenylphosphino)-9,9-dimethyl xanthene (0.092 g, 0.159 mmol, 0.2 equiv) and tris(dibenzylideneacetone) dipalladium (0.073 g, 0.079 mmol, 0.1 equiv) were combined. The reactants were flushed with argon, diluted with dioxane (10 mL) and outfitted with a reflux condenser. The reaction was heated to reflux for 5 hours, then filtered hot and the solvents were evaporated. Silica gel column purification provided desired product as a yellow powder (0.16 g, 39% yield). MS (ESI+): m/z=582.1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481536B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-873234e761ce479092f120292c53c38e
출처 메모uspto-grants-2013_07