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HRID 1749688作成日:2026年10月26日

(S)-3-hydroxybutyric acid → (3S)-1-[4-[5-[5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl]-1-methyl-1,2,4-triazol-3-yl]-1-piperidyl]-3-hydroxy-butan-1-one

https://huagongshe.com/reaction/1749688

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-3-hydroxybutyric acidHCID 94318—
反応物3-(5-tert-butyl-1,3,4-oxadiazol-2-yl)-5-(1-methyl-3-(piperidin-4-yl)-1H-1,2,4-triazol-5-yl)pyrazin-2-amineHCID 86727658—
生成物(3S)-1-[4-[5-[5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl]-1-methyl-1,2,4-triazol-3-yl]-1-piperidyl]-3-hydroxy-butan-1-oneHCID 8672767068.2%

反応手順

Using a similar procedure as Example 4, 3-(5-tert-butyl-1,3,4-oxadiazol-2-yl)-5-(1-methyl-3-(piperidin-4-yl)-1H-1,2,4-triazol-5-yl)pyrazin-2-amine was reacted with (S)-3-hydroxybutanoic acid to afford the title compound (167 mg, 68.2%) as a pale yellow solid. 1H NMR Spectrum: (CDCl3) 1.24 (3H, d), 1.52 (9H, s), 1.85 (2H, m), 2.10 (2H, m), 2.35 (1H, dd), 2.55 (1H, d), 2.90 (1H, m), 3.05 (1H, m), 3.20 (1H, m), 3.90 (1H, m), 4.25 (1H, m), 4.31 (3H, s), 4.6 (1H, m), 9.03 (1H, s); Mass Spectrum [M+H]+=470.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09156831B2
出典データセットuspto-grants-2015_10
ORD IDord-7f152b23aab9477187632f59cee8e69f
出典メモuspto-grants-2015_10