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HRID 16886作成日:2026年10月26日

Acetic Acid → Ethyl 4-(4-cyclopropyl-1,4-diazepan-1-yl)benzoate

https://huagongshe.com/reaction/16886

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Ethyl 4-(1,4-diazepan-1-yl)benzoateHCID 18425301—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 4-(4-cyclopropyl-1,4-diazepan-1-yl)benzoateHCID 66589916118%

反応条件

温度60 °C

反応手順

A solution of ethyl 4-(1,4-diazepan-1-yl)benzoate (0.621 g, 2.5 mmol), (1-ethoxycyclopropoxy)trimethylsilane (2.51 mL, 12.50 mmol) and acetic acid (0.286 mL, 5.00 mmol) in tetrahydrofuran (50 mL), methanol (5 mL) was treated with sodium cyanoborohydride (0.393 g, 6.25 mmol) at 20° C. The resulting solution was stirred at 60° C. for 18 h. The reaction mixture was cooled, filtered and evaporated to dryness. 1N HCl (40 ml) and water (60 ml) were added and the solution extracted with ethyl acetate (3×50 ml). The aqueous layer was basified to pH 10 with solid potassium carbonate and extracted with ethyl acetate (4×50 ml). The organic extracts washed with saturated NaCl (50 ml) and dried over MgSO4, filtered and evaporated to dryness. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 5% MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 4-(4-cyclopropyl-1,4-diazepan-1-yl)benzoate (0.849 g, 118%) as a colourless 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-5ea8033f01d946058fca533261c3438e
出典メモuspto-grants-2010_06