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HRID 370444作成日:2026年10月26日

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

https://huagongshe.com/reaction/370444

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物6-Chloro-7-methyl-[1,2,4]triazolo[4,3-b]pyridazineHCID 819796—
溶媒EthanolHCID 702—
生成物7-Methyl-6-piperidino-s-triazolo[4,3-b]pyridazineHCID 13518811—

反応手順

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.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04526890
出典データセットuspto-grants-1985_07
ORD IDord-c64ff2a37c474fefa41ee9101a711494
出典メモuspto-grants-1985_07