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HRID 732101作成日:2026年10月27日

3-(4-Cyclopropyl-5-pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-2-methyl-acrylic acid ethyl ester → 3-(4-Cyclopropyl-5-pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-2-methyl-propionic acid ethyl ester

https://huagongshe.com/reaction/732101

反応式

関与物質

役割名称HCID仕込み量
反応物3-(4-Cyclopropyl-5-pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-2-methyl-acrylic acid ethyl esterHCID 67070985—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物3-(4-Cyclopropyl-5-pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-2-methyl-propionic acid ethyl esterHCID 57838002—

反応手順

3-(4-cyclopropyl-5-pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-2-methyl-acrylic acid ethyl ester (5.76 g, 19.3 mmol) was hydrogenated with 10% Pd/C (3.0 g) in EtOH (100 ml) o.n. The reaction mixture was filtered and concentrated. The residue was triturated with hex. to give the title compound in 3.1 g (53%) yield. 1H-NMR: 8.76 (d, 2H), 7.73 (d, 2H), 4.14(m, 2H), 3.35 (m, 3H), 2.88 (q, 1H), 1.39 (d, 3H), 1.25 (t, 3H), 1.18 (m, 2H) and 0.73 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07585881B2
出典データセットuspto-grants-2009_09
ORD IDord-8ee6184536884dfdb437ab35dae7039b
出典メモuspto-grants-2009_09