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HRID 229863作成日:2026年10月24日

Methyl acetoacetate → 2-Methyl-1-[(R)-1-(tetrahydro-furan-2-yl)methyl]-5-(2-trifluoromethoxy-phenyl)-1H-pyrrole-3-carboxylic acid cyclohexylamide

https://huagongshe.com/ja/reaction/229863

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CyclohexylamineHCID 7965—
反応物(R)-(-)-TetrahydrofurfurylamineHCID 2734124—
反応物2-(Trifluoromethoxy)phenacyl bromideHCID 2778684—
生成物2-Methyl-1-[(R)-1-(tetrahydro-furan-2-yl)methyl]-5-(2-trifluoromethoxy-phenyl)-1H-pyrrole-3-carboxylic acid cyclohexylamideHCID 11546877—

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-(trifluoromethoxy)phenyl]-ethanone as compound of formula S, (R)-tetrahydrofurfurylamine as R3—(CH2)m—NH2 and cyclohexylamine as R1R2NH, MS (ISP) 451.5 (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-19c79007c6d644dc8efceb46f516b0ed
出典メモuspto-grants-2009_07