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HRID 605811作成日:2026年10月27日

Ethyl Acetate → 3-Pyridyl 4-[4-(cyclooctylmethoxy)benzoyl]-1-piperazinecarboxylate

https://huagongshe.com/reaction/605811

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物CyclooctanemethanolHCID 77196—
反応物DiisopropylethylamineHCID 81531—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物4-(Cyclooctylmethoxy)benzoic acidHCID 57421841—
溶媒DimethylformamideHCID 6228—
生成物3-Pyridyl 4-[4-(cyclooctylmethoxy)benzoyl]-1-piperazinecarboxylateHCID 67067042—

反応手順

1-Ethyl-3-(dimethylaminopropyl)carbodiimide hydrochloride (150 mg), 1-hydroxybenzotriazole (110 mg) and diisopropylethylamine (0.23 ml) were added to a DMF (5 ml) solution containing the resulting compound (190 mg) and 4-(cyclooctylmethoxy)benzoic acid (176 mg) prepared from cyclooctylmethanol with reference to Reference Example 70, followed by stirring overnight at room temperature. The reaction solution was diluted with EtOAc, the organic layer was washed with aqueous saturated sodium hydrogencarbonate solution, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was recrystallized from EtOAc/hexane to obtain 3-pyridyl 4-[4-(cyclooctylmethoxy)benzoyl]-1-piperazinecarboxylate (240 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07915261B2
出典データセットuspto-grants-2011_03
ORD IDord-08f67960fcfb40128f1ed3f5e434b715
出典メモuspto-grants-2011_03