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HRID 927772作成日:2026年10月25日

L-Leucine, N-((1,1-dimethylethoxy)carbonyl)- → 6-[(4-Fluoro-phenyl)-hydroxy-methyl]-pyridine-2-carboxylic acid [(S)-3-methyl-1-(5-methyl-[1,2,4]oxadiazol-3-yl)-butyl]-amide

https://huagongshe.com/reaction/927772

反応式

関与物質

役割名称HCID仕込み量
反応物L-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
反応物6-((4-Fluorophenyl)(hydroxy)methyl)picolinic acidHCID 71087341—
反応物(S)-5-methyl-alpha-(2-methylpropyl)-1,2,4-oxadiazole-3-methanamine hydrochlorideHCID 71087826—
生成物6-[(4-Fluoro-phenyl)-hydroxy-methyl]-pyridine-2-carboxylic acid [(S)-3-methyl-1-(5-methyl-[1,2,4]oxadiazol-3-yl)-butyl]-amideHCID 71105702—

反応手順

The title compound was synthesized in analogy to Example 1, using 6-((4-fluorophenyl)(hydroxy)methyl)picolinic acid and (S)-5-methyl-α-(2-methylpropyl)-1,2,4-oxadiazole-3-methanamine hydrochloride (which was prepared from (2S)-2-[(tert-butoxycarbonyl)amino]-4-methylpentanoic acid (CAN 13139-15-6) in analogy to the procedures described in Example 38 a to e) as starting materials. MS (EI): m/e=399.2 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09290451B2
出典データセットuspto-grants-2016_03
ORD IDord-1db098ee79d3457e8e5e30b18b0541a6
出典メモuspto-grants-2016_03