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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43344생성일: 2026년 10월 24일

Cesium carbonate → 1,1-Dimethylethyl 4-[(3-cyanophenyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/ko/reaction/43344

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참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물3-BromobenzonitrileHCID 23381—
반응물Binap, (A+-)-HCID 634876—
반응물4-Amino-1-Boc-piperidineHCID 1268291—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물1,1-Dimethylethyl 4-[(3-cyanophenyl)amino]-1-piperidinecarboxylateHCID 2522379682.4%

반응 조건

온도105 °C

반응 단계

A mixture of BINAP (560 mg, 0.9 mmol), palladium acetate (135 mg, 0.6 mmol) and cesium carbonate (2.932 g, 9 mmol) in 1,4-dioxane (10 ml) was sonicated for 50 minutes. 1,1-Dimethylethyl 4-amino-1-piperidinecarboxylate (1.2 g, 6 mmol) and 3-bromobenzonitrile (1.638 g, 9 mmol) were added and the mixture heated to 105° C. overnight under an argon atmosphere. On cooling, the solvent was removed in vacuo and the residue partitioned between water (100 ml) and EtOAc (100 ml). The organic layer was separated, dried and concentrated and the crude product purified by chromatography. Elution with a 0-50% Et2O/petroleum ether gradient gave the title compound as a white solid (1.49 g). δH (CDCl3, 250 MHz) 7.22 (2H, t), 6.95 (1H, dd), 6.77 (2H, m), 4.07 (2H, m), 3.77 (1H, m), 3.41 (1H, m), 3.20 (1H, m), 2.93 (2H, m), 2.03 (2H, m), 1.47 (9H, s), 1.34 (2H, m). MS (ES): MH+ 302.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536182B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-9a54a3b366f844a18f94b9db04f87ad0
출처 메모uspto-grants-2013_09