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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2284799생성일: 2026년 10월 26일

tert-Butanol → tert-butyl (2-(4-(2-((3-fluorophenyl)amino)-4-(propylamino)pyrimidin-5-yl)-1H-1,2,3-triazol-1-yl)ethyl)carbamate

https://huagongshe.com/reaction/2284799

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물tert-Butyl (2-azidoethyl)carbamateHCID 22323692—
반응물Sodium AscorbateHCID 23667548—
반응물5-ethynyl-N2-(3-fluorophenyl)-N4-propylpyrimidine-2,4-diamineHCID 90052512—
촉매Copper SulfateHCID 24462—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물tert-butyl (2-(4-(2-((3-fluorophenyl)amino)-4-(propylamino)pyrimidin-5-yl)-1H-1,2,3-triazol-1-yl)ethyl)carbamateHCID 90053341—

반응 단계

To 5-ethynyl-N2-(3-fluorophenyl)-N4-propylpyrimidine-2,4-diamine (S2, 62.4 mg) and tert-butyl(2-azidoethyl)carbamate (S18, 51.6 mg), tert-butanol (0.6 mL), water (0.6 mL), N,N-dimethylformamide (1.2 mL), sodium ascorbate (9.15 mg) and copper sulfate (3.69 mg) were added at room temperature, and the mixture was stirred at the same temperature for 12 hours. To the reaction mixture, ethyl acetate and water were added. The organic layer was separated, washed successively with water and saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain tert-butyl (2-(4-(2-((3-fluorophenyl)amino)-4-(propylamino)pyrimidin-5-yl)-1H-1,2,3-triazol-1-yl)ethyl)carbamate (S19, 32.5 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09145415B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-7d6383cb4844482a88bb92f2310f736c
출처 메모uspto-grants-2015_09