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HRID 16760作成日:2026年10月26日

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

https://huagongshe.com/reaction/16760

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物2-AcetylcyclohexanoneHCID 13400—
反応物Methyl 4-iodobenzoateHCID 69273—
反応物Tert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
触媒Copper iodideHCID 83717—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylateHCID 5736268413.2%

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737149B2
出典データセットuspto-grants-2010_06
ORD IDord-bf580b2f31564622a5397ead6f2f9ef0
出典メモuspto-grants-2010_06