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HRID 229869作成日:2026年10月24日

Methyl acetoacetate → 5-(2-Fluoro-5-trifluoromethyl-phenyl)-2-methyl-1-[(S)-1-(tetrahydro-furan-2-yl)methyl]-1H-pyrrole-3-carboxylic acid ((1R,2R)-2-hydroxy-cyclohexyl)-amide

https://huagongshe.com/ja/reaction/229869

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl acetoacetateHCID 7757—
反応物(S)-(+)-TetrahydrofurfurylamineHCID 641530—
反応物(1R,2R)-2-AminocyclohexanolHCID 735777—
反応物2-Fluoro-5-(trifluoromethyl)phenacyl bromideHCID 2778784—
生成物5-(2-Fluoro-5-trifluoromethyl-phenyl)-2-methyl-1-[(S)-1-(tetrahydro-furan-2-yl)methyl]-1H-pyrrole-3-carboxylic acid ((1R,2R)-2-hydroxy-cyclohexyl)-amideHCID 11669950—

反応手順

The title compound was synthesized in analogy to example 7, using 3-oxo-butyric acid methyl ester as compound of formula R, 2-bromo-1-[2-fluoro-5-(trifluoromethyl)-phenyl]-ethanone as compound of formula S, (S)-tetrahydrofurfurylamine as R3—(CH2)m—NH2 and (1R,2R)-2-aminocyclohexanol as R1R2NH, MS (ISP) 469.5 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07563910B2
出典データセットuspto-grants-2009_07
ORD IDord-37e4ab64492d40c4b96072b351b3e123
出典メモuspto-grants-2009_07