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HRID 1889063作成日:2026年10月26日

3-(4-Pyridinyl)[1,2,4]triazolo[4,3-a]pyrazine → 3-(Pyridin-4-yl)-5,6,7,8-tetrahydro-(1,2,4)triazolo(4,3-a)pyrazine

https://huagongshe.com/reaction/1889063

反応式

関与物質

役割名称HCID仕込み量
反応物3-(4-Pyridinyl)[1,2,4]triazolo[4,3-a]pyrazineHCID 66599235—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物3-(Pyridin-4-yl)-5,6,7,8-tetrahydro-(1,2,4)triazolo(4,3-a)pyrazineHCID 6258769252.4%

反応手順

3-(4-Pyridinyl)[1,2,4]triazolo[4,3-a]pyrazine (538 mg, 2.73 mmol) was hydrogenated under atmospheric hydrogen with 10% Pd/C as a catalyst in ethanol at ambient temperature for 36 hours. The catalyst was filtered off and the solvent was evaporated. The residue was purified on silica gel chromatography using 0-20% of 2M methanol in ammonia—Dichloromethane as eluent to give 3-(4-pyridinyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine (0.288 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08501946B2
出典データセットuspto-grants-2013_08
ORD IDord-07436cf1f0874c7995d3038562c02bd0
出典メモuspto-grants-2013_08