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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 500184생성일: 2026년 10월 26일

Sodium Carbonate → N,N-dimethyl-4-[3-(1-quinolin-6-ylcyclopropyl)imidazo[1,2-a]pyrimidin-6-yl]benzenesulfonamide

https://huagongshe.com/reaction/500184

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Amino-5-bromopyrimidineHCID 231310—
반응물N,N-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1-sulfonamideHCID 3868489—
반응물Chloro(1-quinolin-6-ylcyclopropyl)acetaldehydeHCID 86621504—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매IsopropanolHCID 3776—
생성물N,N-dimethyl-4-[3-(1-quinolin-6-ylcyclopropyl)imidazo[1,2-a]pyrimidin-6-yl]benzenesulfonamideHCID 25144949—

반응 조건

온도120 °C

반응 단계

Sodium carbonate (79.5 mg) in water (0.5 mL) was added to a mixture of N,N-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide (93.4 mg, 0.3 mmol), 5-bromopyrimidin-2-amine (43.5 mg, 0.25 mmol) and tetrakis(triphenylphosphine)palladium (8.7 mg, 0.0075 mmol) in ethanol (1.0 mL) and toluene (1.0 mL). The resulting mixture was heated at 120° C. for 2 h. The mixture was diluted with water, filtered, and washed with water. The solid was collected and dried. Chloro(1-quinolin-6-ylcyclopropyl)acetaldehyde (45.0 mg, 0.183 mmol) in isopropanol (1.0 mL) was added to the above solid. The mixture was heated at 90° C. overnight. After cooling to RT, the mixture was diluted with methanol, and purified by RP-HPLC (pH 10) to give the desired product. LCMS: (M+H)=470.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767675B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-0e0ee58eeef5419aa23b3a0ff5b6b767
출처 메모uspto-grants-2010_08