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HRID 1477503作成日:2026年10月25日

2-Methyltetrahydrofuran → tert-Butyl 1-(3-methyl-1,2,4-oxadiazole-yl)-3-azabicyclo[3.1.0]hexan-3-carboxylate

https://huagongshe.com/reaction/1477503

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethyltetrahydrofuranHCID 7301—
反応物N-HydroxyacetamidineHCID 30926—
反応物Sodium MethoxideHCID 10942334—
反応物Ethyl 3-Boc-3-azabicyclo[3.1.0]hexane-1-carboxylateHCID 53249947—
溶媒WaterHCID 962—
生成物tert-Butyl 1-(3-methyl-1,2,4-oxadiazole-yl)-3-azabicyclo[3.1.0]hexan-3-carboxylateHCID 5848757853.6%

反応手順

2-Methyltetrahydrofuran (15 mL), acetamide oxime (2.54 g, 34.3 mmol) and sodium methoxide (3.70 g, 68.6 mmol) were added to 3-tert-butyl 1-ethyl 3-azabicyclo[3.1.0]hexane-1,3-dicarboxylate (103) (3.5 g, 13.72 mmol) and the mixture was heated to reflux for 20 minutes. Upon cooling the suspension was treated with 60 mL of water and extracted with ethyl acetate (2×50 mL). The combined organics were washed with saturated sodium chloride and dried over magnesium sulfate. The mixture was concentrated and the residue was chromatographed over 20 g of silica gel with hexanes/ethyl acetate; obtained 1.95 g of 104 as a white solid. MS (ESI) m/z 304.0 [M+K]+. 1H NMR (CDCl3) δ: 1.17 (m, 1H), 1.46 (s, 9H), 1.74 (m, 1H), 2.18 (s, 2H), 2.22 (m, 1H), 2.36 (s, 3H), 3.50 (m, 1H), 3.70 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09403806B1
出典データセットuspto-grants-2016_08
ORD IDord-c83c80cf0e7647598bb3f4daa7d94c66
出典メモuspto-grants-2016_08