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HRID 2180168作成日:2026年10月26日

Pyridine → 4-{[2-(3,5-Difluoro-phenyl)-acetylamino]-methyl}-4-(4-iodo-phenyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2180168

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2-(3,5-Difluorophenyl)acetyl chlorideHCID 2782723—
反応物4-Aminomethyl-4-(4-iodo-phenyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 20779474—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物4-{[2-(3,5-Difluoro-phenyl)-acetylamino]-methyl}-4-(4-iodo-phenyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 6853060465%

反応手順

To a stirred solution of 4-aminomethyl-4-(4-iodo-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (0.10 g, 0.24 mmol) in CH2Cl2 (0.5 mL) at room temperature under Ar was added a solution of 3,5-difluorophenylacetyl chloride (0.28 mL of a 1 M solution in CH2Cl2, 0.28 mmol) followed by pyridine (0.25 mL). The mixture was stirred at room temperature for 16 h then diluted with EtOAc (5 mL) and washed with saturated aqueous NaHCO3 (5 mL) and saturated brine (5 mL) and dried over Na2SO4. Filtration and rotary evaporation gave the crude 4-{[2-(3,5-difluoro-phenyl)-acetylamino]-methyl}-4-(4-iodo-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (0.09 g, ˜65%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06887889B2
出典データセットuspto-grants-2005_05
ORD IDord-7fb6fa4cdbfd4836927113bae9a372fd
出典メモuspto-grants-2005_05