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HRID 720190作成日:2026年10月25日

4-Methylmorpholine → HCID 69745735、化合物

https://huagongshe.com/reaction/720190

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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物(2S)-1-((tert-butoxy)carbonyl)azetidine-2-carboxylic acidHCID 2734495—
反応物HCID 21901549HCID 21901549—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 69745735HCID 69745735—

反応条件

温度0 °C

反応手順

2-{4-[2-Amino-3-(4-fluorophenyl)-propionyl]-3-ethyl-piperazin-1-yl}-N-methyl-3-naphthalen-2-yl-propioamide, 41, (0.78 g, 0.83 mmol) and Boc-L-azetidine-2-carboxylic acid (0.17 g, 0.83 mmol), 1-(3-dimethylamino-propyl)-3-ethylcarbodiimide (0.19 g, 1.0 mmol) and 1-hydroxybenzotriazole (0.22 g, 1.66 mmol) are dissolved in anhydrous DMF (2 mL). The reaction mixture is cooled to 0° C., then N-methylmorpholine (0.6 mL, 5.46 mmol) is added. The reaction mixture is stirred for 4 hrs. EtOAc (30 mL) and water (100 mL) are added, and the organic layer is separated. The aqueous layer is extracted with EtOAc (3×30 mL). All organic layers are combined and washed with water (2×50 mL), and dried over Na2SO4. The solution is concentrated in vacuo to afford the desired product which is used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07132539B2
出典データセットuspto-grants-2006_11
ORD IDord-1a8374bcb701416987c200ee7c47e329
出典メモuspto-grants-2006_11