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HRID 427669作成日:2026年10月26日

Dimethylformamide → N1-(4-Difluoromethoxybenzoyl)-N2-[1-(4-pyridyl)piperidin-4-ylmethoxycarbonyl]-1,2-benzenediamine Hydrochloride

https://huagongshe.com/reaction/427669

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物4-(Difluoromethoxy)benzoic acidHCID 737360—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物N2-[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl-1,2-benzenediamineHCID 10829995—
生成物N1-(4-Difluoromethoxybenzoyl)-N2-[1-(4-pyridyl)piperidin-4-ylmethoxycarbonyl]-1,2-benzenediamine HydrochlorideHCID 8675756138%

反応手順

To a solution of N1-[1-(4-pyridyl)piperidin-4-yl-methoxycarbonyl]-1,2-benzenediamine (0.2 g, 0.6 mmol) and 4-difluoromethoxybenzoic acid (0.23 g, 1.2 mmol) in DMF (10 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.24 g, 1.2 mmol). After stirring overnight, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate (300 mL) and 1 N NaOH (150 ml). The layers were separated and the organic phase was washed with brine, dried with MgSO4, filtered and concentrated in vacuo. The residue was purified by RPHPLC method A and the fractions containing pure product were combined and lypholized to give 123 mg (38%) of the title product as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313122B1
出典データセットuspto-grants-2001_11
ORD IDord-ede4f5886f7c4bdca988094cfef1c0e2
出典メモuspto-grants-2001_11