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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 713450생성일: 2026년 10월 26일

(2,3-Dihydro-1-benzofuran-5-yl)boronic acid → 4-(2,3-Dihydro-benzofuran-5-carbonyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/713450

반응식

참여 물질

역할이름HCID투입량
반응물(2,3-Dihydro-1-benzofuran-5-yl)boronic acidHCID 2773380—
반응물4-Phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl esterHCID 89375800—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매Cuprous 2-thiophenecarboxylateHCID 11194830—
용매1,2-DimethoxyethaneHCID 8071—
생성물4-(2,3-Dihydro-benzofuran-5-carbonyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 7122696089.7%

반응 단계

To a mixture of 2,3-dihydro-1-benzofuran-5-ylboronic acid (0.56 g, 1.56 mmol), ligand TFP (0.07 g, 0.3 mmol), Pd2dba3 (0.28 g, 0.30 mmol), copper (I) thiophene-2-carboxylate (0.45 g, 2.4 mmol) was added a solution of 4-phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl ester (0.5 g, 1.6 mmol) in 15 mL of DME 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 (0.5 g, 1.4 mmol). MS (ESI) m/z 331.8 (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 1.54 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181266B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-b3577d2216d948c5a6828cf2c7397f73
출처 메모uspto-grants-2015_11