関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Levodopa | HCID 6047 | — |
| 反応物 | Acetyl chloride | HCID 6367 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Melevodopa | HCID 23497 | 117.3% |
反応手順
A 3-Liter three-necked round-bottom flask equipped with a cooling bath, a thermometer and a condenser was charged with 1.5 Liters methanol, and acetyl chloride (119 ml, 1.2 mol) was carefully added thereto at 0° C. The cooling bath was replaced with a heating mantle and the mixture was heated to 15° C. 60 grams (0.3 mol) of L-3-(3,4-dihydroxy-phenyl)alanine was then added and the reaction mixture was refluxed for 3 hours and thereafter concentrated under reduced pressure at 60° C. to afford 74.3 grams (100% yield) of Compound 2 (see, Scheme 1). The product structure was confirmed by 1H-NMR.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08207369B2 |
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| 出典データセット | uspto-grants-2012_06 |
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| ORD ID | ord-4a47b9208e444a0f9d11a7aa6fff6a61 |
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| 出典メモ | uspto-grants-2012_06 |
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