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HRID 43339作成日:2026年10月23日

Acetic Acid → tert-Butyl 4-(3-fluoroanilino)piperidine-1-carboxylate

https://huagongshe.com/ja/reaction/43339

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3-FluoroanilineHCID 9742—
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
溶媒DichloromethaneHCID 6344—
生成物tert-Butyl 4-(3-fluoroanilino)piperidine-1-carboxylateHCID 2313759182%

反応手順

A solution of 1,1-dimethylethyl 4-oxo-1-piperidinecarboxylate (1.91 g, 9.53 mmol), 3-fluoroaniline (1.06, 9.53 mmol) and acetic acid (0.55 ml, 9.53 mmol) in 1,2-DCE (50 ml) was stirred at room temperature overnight. Sodium tri(acetoxy)borohydride (2.82 g, 13.3 mmol) was then added, stirred for 8 hrs and then allowed to stand at room temperature. The reaction mixture was diluted with DCM and washed with NaHCO3 solution, dried over MgSO4 and then concentrated to give the product which was purified by column chromatography. Elution with 0-40% EtOAc/pentane gave the title compound as a white solid (2.3 g). δH (CDCl3, 250 MHz) 7.08 (1H, q), 6.35 (3H, m), 4.04 (1H, br s), 3.65 (1H, br s), 3.38 (1H, m), 2.92 (2H, m), 2.02 (2H, m), 1.47 (9H, s), 1.34 (2H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536182B2
出典データセットuspto-grants-2013_09
ORD IDord-ed5e4844a6594da5b9d1c7dabd6a94e7
出典メモuspto-grants-2013_09