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HRID 16717作成日:2026年10月26日

1,2-Ethanediamine, N1,N1,N2-trimethyl- → HCID 178501159、化合物

https://huagongshe.com/reaction/16717

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Sodium BicarbonateHCID 516892—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物HCID 178501163HCID 178501163—
溶媒ChloroformHCID 6212—
生成物HCID 178501159HCID 17850115993.3%

反応手順

Trans-4-(methoxycarbonyl)cyclohexanecarboxylic acid (8.84 g) obtained in Reference Example 1(2) is dissolved in chloroform (100 ml), and thereto are added 1-hydroxybenzotriazole (7.14 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (10.00 g) and N,N,N′-trimethylethylenediamine (5.33 g) under ice-cooling. The mixture is then stirred at room temperature for 4 hours. Saturated aqueous sodium hydrogen carbonate solution is poured to the reaction solution and the mixture is extracted with chloroform. The organic layer is washed with saturated brine and dried over sodium sulfate. The solvent is concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (eluent: chloroform/methanol/28% ammonia water=200/10/1) to give methyl trans-4-{[[2-(dimethylamino)ethyl](methyl)amino]carbonyl}-cyclohexanecarboxylate (11.98 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737161B2
出典データセットuspto-grants-2010_06
ORD IDord-8b58af24ecdb470eb2de945d1ee82651
出典メモuspto-grants-2010_06