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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40195생성일: 2026년 10월 23일

Sodium Iodide → N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7-(2-(pyrrolidin-1-yl)ethoxy)-1,5-naphthyridin-4-amine

https://huagongshe.com/ko/reaction/40195

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Cesium carbonateHCID 10796—
반응물1-(2-Chloroethyl)pyrrolidine hydrochlorideHCID 81668—
반응물8-((6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylamino)-1,5-naphthyridin-3-olHCID 135987478—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물Ammonium hydroxide methanolHCID 21894508—
생성물N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7-(2-(pyrrolidin-1-yl)ethoxy)-1,5-naphthyridin-4-amineHCID 5769130122.2%

반응 조건

온도75 °C

반응 단계

In a 10 mL sealed tube under N2 were dissolved CESIUM CARBONATE (221 mg, 677 μmol), 8-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylamino)-1,5-naphthyridin-3-ol (50 mg, 135 μmol), 1-(2-chloroethyl)pyrrolidine hydrochloride (46 mg, 271 μmol) and SODIUM IODIDE (41 mg, 271 μmol) in 1 mL of DMSO then stirred and heated at 75° C. for 3 h. The reaction mixture was diluted with H2O and the aqueous phase was extracted 3× with DCM then the organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The crude mixture was purified by MPLC (ISCO) with DCM/DCM:MeOH:NH4OH (90:10:1)100:0 to 90:10 to afforded N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7-(2-(pyrrolidin-1-yl)ethoxy)-1,5-naphthyridin-4-amine (7 mg, 11% yield) as a yellow solid. MS m/z=466.2 [M+1]+. Calc'd for C26H26N8O: 467.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-bbfaf995e8d949f080af9e7cd0b469b2
출처 메모uspto-grants-2013_09