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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75991생성일: 2026년 10월 24일

4-(2-Methylbutan-2-yl)benzene-1-sulfonyl chloride → n-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1,1-dimethyl-propyl)-benzenesulfonamide

https://huagongshe.com/ko/reaction/75991

반응식

참여 물질

역할이름HCID투입량
반응물4-(2-Methylbutan-2-yl)benzene-1-sulfonyl chlorideHCID 22281976—
반응물4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenylamineHCID 59428114—
용매PyridineHCID 1049—
생성물n-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1,1-dimethyl-propyl)-benzenesulfonamideHCID 25135042—

반응 단계

A 4 mL scintillation vial was charged with 4-chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenylamine (100 mg, 0.363 mmol), 4-(1,1-dimethyl-propyl)-benzenesulfonyl chloride (98 g, 0.399 mmol), and pyridine (1 mL). The resultant solution was stirred 4 hours at 80° C. and then partitioned with EtOAc/1 M HCl. The organics were subsequently washed with 1 M HCl, saturated aqueous sodium bicarbonate, and brine; dried over anhydrous sodium sulfate; and removed in vacuo. The resultant residue was then purified via automated silica gel chromatography to afford the desired sulfonamide: MS (ES) M+H expected 456.2, found 456.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835468B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-675f9c9f37914158a540573c6559152c
출처 메모uspto-grants-2014_09