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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Methyltetrahydrofuran | HCID 7301 | — |
| 反応物 | N-Hydroxyacetamidine | HCID 30926 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | Ethyl 3-Boc-3-azabicyclo[3.1.0]hexane-1-carboxylate | HCID 53249947 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | tert-Butyl 1-(3-methyl-1,2,4-oxadiazole-yl)-3-azabicyclo[3.1.0]hexan-3-carboxylate | HCID 58487578 | 53.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09403806B1 |
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| 出典データセット | uspto-grants-2016_08 |
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| ORD ID | ord-c83c80cf0e7647598bb3f4daa7d94c66 |
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| 出典メモ | uspto-grants-2016_08 |
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