戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 251382作成日:2026年10月27日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Ethyl 3-{[2-(4-morpholinyl)ethyl]oxy}benzoate

https://huagongshe.com/reaction/251382

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物tert-Butyl carbazateHCID 70091—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物3-(5-amino-4-benzoyl-1H-pyrazol-1-yl)-4-methylbenzoic acidHCID 11209438—
反応物Sodium chloride; waterHCID 57417360—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 3-{[2-(4-morpholinyl)ethyl]oxy}benzoateHCID 5808903926%

反応条件

温度0 °C

反応手順

To DMF (10 mL) at rt was added 3-(5-amino-4-benzoyl-pyrazol-1-yl)-4-methyl-benzoic acid 1 (0.50 g, 1.56 mmol, 1.0 eq), t-butylcarbazate (0.206 g, 1.56 mmol, 1.0 eq), EDCI (0.313 g, 1.63 mmol, 1.05 eq) and HOBt (0.238 g, 1.56 mmol, 1.0 eq). The reaction was stirred for 19 h, poured into brine (100 mL) and extracted with EtOAc (2×20 mL). The organic extracts were combined were washed with brine (1×20 mL). The brine layer was separated and extacted with EtOAc (1×10 mL). All organic extracts were combined dried over Na2SO4, filtered and concentrated in vacuo. This material was dissolved in CH2Cl2 (10 mL) and cooled to 0° C. TFA (3 mL) was added and the reaction mixture allowed to warm to rt over 2 h. The solvent was removed in vacuo to give crude solid which was triturated with EtOAc/ether (1/1) giving 2 (180 mg, 26%)as a light tan in color solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863314B2
出典データセットuspto-grants-2011_01
ORD IDord-01c92dc9ae754fbfa8ce639352e63b35
出典メモuspto-grants-2011_01