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HRID 1845170作成日:2026年10月26日

Diisopropylethylamine → Ethyl 4'-methyl-5-((2-methylpyrimidin-5-yl)methylcarbamoyl)biphenyl-3-carboxylate

https://huagongshe.com/reaction/1845170

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物(2-Methylpyrimidin-5-yl)methanamineHCID 21294601—
反応物5-(Ethoxycarbonyl)-4'-methylbiphenyl-3-carboxylic acidHCID 58187957—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium BicarbonateHCID 516892—
生成物Ethyl 4'-methyl-5-((2-methylpyrimidin-5-yl)methylcarbamoyl)biphenyl-3-carboxylateHCID 44223019—

反応手順

To a mixture of crude 5-(ethoxycarbonyl)-4′-methylbiphenyl-3-carboxylic acid (450 mg, 1.6 mmol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (610 mg, 3.2 mmol), 1-hydroxybenzotriazole hydrate (240 mg, 1.6 mmol), CH2Cl2 (5 mL) were added (2-methylpyrimidin-5-yl)methanamine (290 mg, 2.4 mmol) and N,N-diisopropylethylamine (0.41 mL, 2.4 mmol). The reaction mixture was stirred at room temperature overnight, and then diluted with aq. NaHCO3 solution and EtOAc (100 mL). The organic layer was separated, washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column (0-20% MeOH/CH2Cl2) to afford the title product as a white foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08946439B2
出典データセットuspto-grants-2015_02
ORD IDord-97d7561a4eaa4f94bb3082982c572994
出典メモuspto-grants-2015_02