関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1,3-Benzodioxol-4-ol | HCID 586727 | — |
| 反応物 | 4-(2-Butynyloxy)-6-chloropyrimidine | HCID 12137602 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-(2-Butynyloxy)-6-(2,3-methylenedioxyphenoxy)pyrimidine | HCID 22599783 | 68% |
反応手順
To 2 ml of N,N-dimethylformamide were added 183 mg of 4-chloro-6-(2-butynyloxy)pyrimidine, 166 mg of potassium carbonate, and 138 mg of 2,3-methylenedioxyphenol, followed by stirring at 80° C. for 7 hours and then at 120° C. for 3 hours. The reaction mixture was then left for cooling to room temperature and subjected to phase separation three times between ethyl acetate and an aqueous sodium chloride solution. The organic layers were dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography to give 193 mg of 4-(2-butynyloxy)-6-(2,3-methylenedioxyphenoxy)pyrimidine (the present compound (64)).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06838463B2 |
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| 出典データセット | uspto-grants-2005_01 |
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| ORD ID | ord-7f7c8712b8194b05b70f7c69377106d9 |
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| 出典メモ | uspto-grants-2005_01 |
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