関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Carbonic acid-guanidine (1:1) | HCID 286947 | — |
| 反応物 | Ethyl 3-(furan-2-yl)-2-methyl-3-oxopropanoate | HCID 12143105 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-amino-6-furan-2-yl-5-methyl-3H-pyrimidin-4-one | HCID 135402458 | 123.1% |
反応手順
Following the method of Rorig and Nicholson (U.S. Pat. No. 2,710,867), a mixture of 3.00 g (15.3 mmol) (RS)-3-furan-2-yl-2-methyl-3-oxo-propionic acid ethyl ester and 1,38 g (7.65 mmol) guanidine carbonate in 20 ml ethanol was heated at 100° C. for 16 hours. The reaction mixture was then cooled to 0° C., whereupon the resulting crystals were collected by filtration and washed sequentially with water and with ice-cold ethanol to afford 1.80 g (62%) 2-amino-6-furan-2-yl-5-methyl-3H-pyrimidin-4-one as a white crystalline solid. ES-MS m/e (%): 190 ([M—H]−, 100).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06586441B2 |
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| 出典データセット | uspto-grants-2003_07 |
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| ORD ID | ord-e8151700ff21411b83c9c3d79e7486d6 |
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| 出典メモ | uspto-grants-2003_07 |
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