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HRID 1753913作成日:2026年10月25日

Diisopropylethylamine → HCID 70816785、化合物

https://huagongshe.com/reaction/1753913

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trans-2-Aminomethyl-1-cyclohexanolHCID 2724658—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物HCID 70817044HCID 70817044—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
溶媒Ammonium ChlorideHCID 25517—
生成物HCID 70816785HCID 7081678563%

反応手順

To a solution of 2-isopropyl-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid (synthesized similar to the methods described in sections a) to d) of example X1) (0.20 g, 0.76 mmol) in dichloromethane (15 ml) are added N-ethyl-diisopropylamine (0.32 ml, 0.89 mmol), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.17 g, 0.91 mmol), and 1-hydroxybenzotriazole hydrate (0.02 g, 0.15 mmol). The mixture is stirred for 15 min at RT, and then cooled to 0° C., before (1R,2S)-2-(aminomethyl)cyclohexanol (0.09 g, 0.76 mmol) is added and stirring is continued for 18 h. After completion of the reaction, the mixture is diluted with ethyl acetate and 10% aqueous ammonium chloride. The organic layer is separated and washed with saturated sodium hydrogencarbonate solution and brine, dried over magnesium sulphate and evaporated to dryness. The crude product is purified by flash chromatography (silica gel, 50% ethyl acetate/cyclohexane) to yield N-[[(1S,2R)-2-hydroxy-cyclohexyl]-methyl]-2-isopropyl-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide (example X7) (0.18 g, 0.48 mmol, 63%). [M+H]+376.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09168259B2
出典データセットuspto-grants-2015_10
ORD IDord-eabe245b6376419ebe490432d8fc37e4
出典メモuspto-grants-2015_10