戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 17101作成日:2026年10月25日

Dimethylformamide → HCID 57393214、化合物

https://huagongshe.com/reaction/17101

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Trifluoroacetic acidHCID 6422—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物DiisopropylethylamineHCID 81531—
反応物3-Methoxypropionic acidHCID 134442—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物HCID 57393214HCID 57393214—

反応手順

To a mixture of A215 (0.020 g, 0.065 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.019 g, 0.098 mmol), 1-hydroxybenzotriazole (0.013 g, 0.098 mmol), and diisopropylethylamine (0.034 mL, 0.195 mmol) in anhydrous dimethylformamide (2 mL) was added 3-methoxypropionic acid (9.20 μL, 0.098 mmol). The reaction mixture was stirred at room temperature overnight (After ˜3 hr, the reaction mixture became homogenous). The solvent was removed under reduced pressure, and the residue was diluted with dichloromethane, washed with water, and dried over anhydrous sodium sulfate. Concentration under pressure followed by purification by flash silica gel chromatography using a 5% mixture of methanol in dichloromethane afforded 0.018 g (69%) of A216 as a yellow solid. The compound had an HPLC retention time=1.84 min. (Column: Chromolith SpeedROD 4.6×50 mm—4 min.; Solvent A=10% MeOH, 90% H2O, and 0.1% TFA; Solvent B=90% MeOH, 10% H2O, and 0.1% TFA) and a LC/MS M+1=394.37. 1H NMR (400 MHz, CDCl3) δ ppm 2.62 (t, J=7.15 Hz, 2 H) 3.15 (d, J=6.60 Hz, 3 H) 3.54 (s, 3 H) 3.78 (t, J=7.15 Hz, 2 H) 4.01 (s, 3 H) 4.56 (d, J=6.10 Hz, 2 H) 5.49-5.54 (m, 1 H) 6.96-6.98 (m, 2 H) 7.51-7.58 (m, 3 H) 9.98 (s, 1 H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737279B2
出典データセットuspto-grants-2010_06
ORD IDord-143b8358ec3a4888b04d3d892bb7d06c
出典メモuspto-grants-2010_06