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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1182056생성일: 2026년 10월 27일

Hydrochloric Acid → 5-[5-Bromo-4-(4-hydroxy-butylsulfanyl)-pyrimidin-2-ylamino]-pyridine-2-sulfonic acid amide

https://huagongshe.com/reaction/1182056

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물5-Aminopyridine-2-sulfonamideHCID 22313850—
반응물4-(5-Bromo-2-chloro-pyrimidin-4-ylsulfanyl)-butan-1-olHCID 58981899—
용매EthanolHCID 702—
용매AcetonitrileHCID 6342—
용매1,4-DioxaneHCID 31275—
생성물5-[5-Bromo-4-(4-hydroxy-butylsulfanyl)-pyrimidin-2-ylamino]-pyridine-2-sulfonic acid amideHCID 58981837—

반응 단계

298 mg (1.0 mmol) of 4-(5-bromo-2-chloro-pyrimidin-4-ylsulfanyl)-butan-1-ol is dissolved in 2 ml of acetonitrile and added to a suspension of 172 mg (1.0 mmol) of 5-amino-pyridine-2-sulfonic acid amide (representation according to W. T. Caldwell, E. C. Kornfeld J Am. Chem. Soc. 1942, 64, 1695-1698) in 1 ml of acetonitrile, 0.25 ml of a 4 molar solution of hydrochloric acid in 1,4-dioxane as well as 0.25 ml of water. The reaction mixture is stirred under reflux for 24 hours. It is mixed with 1 ml of ethanol and stirred for another 24 hours under reflux. After cooling, the precipitate that is formed is filtered off, and the filtrate is concentrated by evaporation. The residue is purified by chromatography (Flashmaster II, DCM/MeOH 9:1). The crude product that is obtained is then purified by preoperative thin-layer chromatography. 43 mg (0.10 mmol, 10% of theory) of the product 5-[5-bromo-4-(4-hydroxy-butylsulfanyl)-pyrimidin-2-ylamino]-pyridine-2-sulfonic acid amide is obtained

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07288547B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-8d84815d3e5543c283b1d91b213055dd
출처 메모uspto-grants-2007_10