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HRID 49556作成日:2026年10月24日

4-Methylmorpholine → 4-(Aminosulfonyl)-N-((cis)-2-{[({[2-(trifluoromethyl)anilino]carbonyl)amino)acetyl]amino}cyclohexyl)benzamide

https://huagongshe.com/ja/reaction/49556

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物Ethyl AcetateHCID 8857—
反応物2-(Trifluoromethyl)phenyl isocyanateHCID 16794—
反応物N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromideHCID 68830145—
溶媒DimethylformamideHCID 6228—
生成物4-(Aminosulfonyl)-N-((cis)-2-{[({[2-(trifluoromethyl)anilino]carbonyl)amino)acetyl]amino}cyclohexyl)benzamideHCID 68826663—

反応手順

N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide, (61b), (100 mg) was dissolved in DMF (3 mL) prior to the addition of 4-methylmorpholine (0.13 mL) and 2-trifluoromethylphenyl isocyanate (0.05 mL). After stirring overnight, EtOAc was added and the solution was washed with 1N HCl. The EtOAc was dried, filtered, and concentrated. Reverse phase HPLC purification (gradient elution, water/acetonitrile/TFA) of the resulting residue provided the title benzamide (50 mg). MS found: (M+Na)+=564.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706712B2
出典データセットuspto-grants-2004_03
ORD IDord-548d4312cc224e57adc1d3f3ab1ca060
出典メモuspto-grants-2004_03