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HRID 1674914作成日:2026年10月27日

6-Piperazino-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine → N-[3-[[4-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]phenyl]methanesulfonamide

https://huagongshe.com/reaction/1674914

反応式

関与物質

役割名称HCID仕込み量
反応物6-Piperazino-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazineHCID 1476862—
反応物N-(3-formylphenyl)methanesulfonamideHCID 2794787—
生成物N-[3-[[4-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]phenyl]methanesulfonamideHCID 67340018—

反応手順

Reductive amination of 6-(piperazin-1-yl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine with N-(3-formylphenyl)methanesulfonamide was carried out according to General Synthetic Method 7. The crude product was purified by hplc using a Waters XBridge Prep C18 OBD column, 5μ silica, 30 mm diameter, 100 mm length eluted with decreasingly polar mixtures of water (containing 0.1% aqueous ammonia) and acetonitrile as eluents to give N-[3-[[4-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]phenyl]methanesulfonamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08003649B2
出典データセットuspto-grants-2011_08
ORD IDord-32731144e3524beb8b4bae73311800f5
出典メモuspto-grants-2011_08