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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370444생성일: 2026년 10월 26일

Piperidine → 7-Methyl-6-piperidino-s-triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/370444

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물6-Chloro-7-methyl-[1,2,4]triazolo[4,3-b]pyridazineHCID 819796—
용매EthanolHCID 702—
생성물7-Methyl-6-piperidino-s-triazolo[4,3-b]pyridazineHCID 13518811—

반응 단계

7.8 Grams (0.0462 mole) of the 6-chloro-7-methyl-s-triazolo[4,3-b]pyridazine is mixed with 7.86 grams (0.0924 mole) of piperidine in 50 ml of ethanol. The mixture is heated at reflux temperature for 4 hours. The mixture is concentrated by evaporation and the residue of the reaction mixture is partitioned between aqueous sodium bicarbonate solution and methylene chloride. The methylene chloride layer is separated, dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The 7-methyl-6-piperidino-s-triazolo[4,3-b]pyridazine product is obtained as a residue from the evaporation. The product is recrystallized from hexane and found to melt at 78°-79° C. The structure of the product is confirmed by infrared spectroscopy, by nuclear magnetic resonance analysis, and by elemental analysis. (Calculated for C11H15N5 : C, 60.80; H, 6.96; N, 32.24. Found: C, 60.40; H, 6.98; N, 32.17.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04526890
출처 데이터셋uspto-grants-1985_07
ORD IDord-c64ff2a37c474fefa41ee9101a711494
출처 메모uspto-grants-1985_07