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HRID 713458作成日:2026年10月26日

3-Chloro-4-methoxybenzeneboronic acid → 4-(3-Chloro-4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butylester

https://huagongshe.com/reaction/713458

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-methoxybenzeneboronic acidHCID 3247522—
反応物4-Phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl esterHCID 89375800—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
触媒Cuprous 2-thiophenecarboxylateHCID 11194830—
溶媒TetrahydrofuranHCID 8028—
生成物4-(3-Chloro-4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butylesterHCID 7123607888.4%

反応手順

To a mixture of 3-chloro-4-methoxyphenylboronic acid (0.87 g, 4.67 mmol), ligand TFP (0.14 g, 0.6 mmol), Pd2dba3 (0.29 g, 0.31 mmol), copper (I) thiophene-2-carboxylate (0.89 g, 4.7 mmol) was added a solution of 4-phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl ester (1.0 g, 3.1 mmol) in 10 mL of THF while purging with N2 at 50° C. After 18 hours the reaction mixture was diluted with ethyl acetate, filtered through celite then concentrated in vacuo. Purification by flash chromatography gave the title compound (1.02 g, 2.74 mmol). MS (ESI) m/z 354.0 (M+H+); HPLC (Novapak 150×3.9 mm C-18 column: mobile phase: 35-90% acetonitrile/water with 0.1% TFA, at 2 mL/min over 2 min.) t 1.42 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181266B2
出典データセットuspto-grants-2015_11
ORD IDord-f5519f890ff84bf9bf6ab184dfd0df64
出典メモuspto-grants-2015_11