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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 713458생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/713458

반응식

참여 물질

역할이름HCID투입량
반응물3-Chloro-4-methoxybenzeneboronic acidHCID 3247522—
반응물4-Phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl esterHCID 89375800—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매Cuprous 2-thiophenecarboxylateHCID 11194830—
용매TetrahydrofuranHCID 8028—
생성물4-(3-Chloro-4-methoxy-benzoyl)-piperidine-1-carboxylic acid tert-butylesterHCID 7123607888.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181266B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-f5519f890ff84bf9bf6ab184dfd0df64
출처 메모uspto-grants-2015_11