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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16760생성일: 2026년 10월 24일

Cesium carbonate → Tert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylate

https://huagongshe.com/ko/reaction/16760

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참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-AcetylcyclohexanoneHCID 13400—
반응물Methyl 4-iodobenzoateHCID 69273—
반응물Tert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
촉매Copper iodideHCID 83717—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylateHCID 5736268413.2%

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온도90 °C

반응 단계

Methyl 4-iodobenzoate (1.00 g, 3.82 mmol, 1.0 eq) was dissolved in DMF and tert-butyl 1,4-diazepane-1-carboxylate (765 mg, 3.82 mmol, 1.0 eq), caesium carbonate (2.49 g, 7.63 mmol, 2.0 eq), 2-acetylcyclohexanone (101 μl, 0.76 mmol, 0.20 eq [20 mol %]) and copper iodide (37 mg, 0.19 mmol, 0.05 eq [5 mol %]) were added. The reaction mixture was stirred at 90° C. under nitrogen for 7 h. The reaction mixture was evaporated, dissolved in DCM (50 ml), washed with water (20 ml), saturated ammonium chloride solution (20 ml), dried over MgSO4, filtered and evaporated. The crude product was purified by silica column chromatography, eluting with 0-1% MeOH in DCM. The product containing fractions were combined, evaporated and dried in vacuo to give tert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylate (168 mg, 13%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737149B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-bf580b2f31564622a5397ead6f2f9ef0
출처 메모uspto-grants-2010_06