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HRID 405749作成日:2026年10月23日

5-Cyanopyridine-2-carboxylic acid → N-{3-[(4r,5s)-2-Amino-5-Fluoro-4-Methyl-5,6-Dihydro-4h-1,3-Oxazin-4-Yl]-4-Fluorophenyl}-5-Cyanopyridine-2-Carboxamide

https://huagongshe.com/ja/reaction/405749

反応式

関与物質

役割名称HCID仕込み量
反応物5-Cyanopyridine-2-carboxylic acidHCID 12400734—
反応物(4R,5S)-4-(5-amino-2-fluoro-phenyl)-5-fluoro-4-methyl-5,6-dihydro-4H-[1,3]oxazin-2-ylamineHCID 86672005—
生成物N-{3-[(4r,5s)-2-Amino-5-Fluoro-4-Methyl-5,6-Dihydro-4h-1,3-Oxazin-4-Yl]-4-Fluorophenyl}-5-Cyanopyridine-2-CarboxamideHCID 66558858—

反応手順

The condensation of (4R,5S)-4-(5-amino-2-fluoro-phenyl)-5-fluoro-4-methyl-5,6-dihydro-4H-[1,3]oxazin-2-ylamine (intermediate A8.1) and 5-cyano-pyridine-2-carboxylic acid following procedure I yielded the title compound as a white solid. MS (ISP): m/z=372.2 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754075B2
出典データセットuspto-grants-2014_06
ORD IDord-828919b68cfb48a8aa57e8de1513a633
出典メモuspto-grants-2014_06