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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273527생성일: 2026년 10월 26일

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/273527

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—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
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 번호US07456176B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-e298ff2894a24f038612b2965fef1faa
출처 메모uspto-grants-2008_11