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HRID 1045803作成日:2026年10月27日

1,2-Dichloroethane → Benzyl 4-[(4-chloro-3-methyl-phenyl)carbamoyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/1045803

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物4-Chloro-3-methylanilineHCID 23536—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 736489—
溶媒DichloromethaneHCID 6344—
生成物Benzyl 4-[(4-chloro-3-methyl-phenyl)carbamoyl]piperidine-1-carboxylateHCID 86685835—

反応手順

1-Benzyloxycarbonylpiperidine-4-carboxylic acid (1.00 g, 3.80 mmol) and 4-chloro-3-methyl-aniline (0.592 g, 4.18 mmol) in CH2Cl2 (5 mL) were treated with HOBT (0.582, 3.80 mmol) and EDC (1.46 g, 7.60 mmol), and stirred at rt for 16 h. The mixture was directly purified on SiO2 (50 to 100% EtOAc, hexanes) to afford the title compound. HPLC/MS: 387.2/389.1 (M+1); Rt=1.22 min (LC2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569299B2
出典データセットuspto-grants-2013_10
ORD IDord-7b429f0b596b4ec1a27a93606eb29940
出典メモuspto-grants-2013_10