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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | 5-Aminopyridine-2-sulfonamide | HCID 22313850 | — |
| 반응물 | 4-(5-Bromo-2-chloro-pyrimidin-4-ylsulfanyl)-butan-1-ol | HCID 58981899 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 5-[5-Bromo-4-(4-hydroxy-butylsulfanyl)-pyrimidin-2-ylamino]-pyridine-2-sulfonic acid amide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07288547B2 |
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| 출처 데이터셋 | uspto-grants-2007_10 |
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| ORD ID | ord-8d84815d3e5543c283b1d91b213055dd |
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| 출처 메모 | uspto-grants-2007_10 |
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