関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | Dopamine Hydrochloride | HCID 65340 | — |
| 反応物 | N-Hydroxysuccinimide | HCID 80170 | — |
| 反応物 | (+-)-3,4-Dihydroxymandelic acid | HCID 85782 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | N-(3,4-dihydroxyphenethyl)-2-(3,4-dihydroxyphenyl)-2-hydroxyacetamide | HCID 9797093 | — |
反応手順
2-(3,4-Dihydroxyphenyl)-2-hydroxyacetic acid (300 mg, 1.63 mmol) and N-hydroxysuccinimide (188 mg, 1.63 mmol) were dissolved in 1,4-dioxane (20 ml) under nitrogen, and N,N′-dicyclohexylcarbodiimide (336 mg, 1.63 mmol) was added to the mixture at room temperature, which was stirred at this temperature for 16 h. The by-product which precipitated out was filtered off, and the filtrate was added to a solution of 2-(3,4-dihydroxyphenyl)ethylamine hydrochloride (309 mg, 1.63 mmol) in water (20 ml). Sodium hydrogencarbonate (151 mg, 1.8 mmol) was also added, and the reaction mixture was stirred under nitrogen at 50° C. for 1.5 h. The mixture was rendered acidic using 5% strength hydrochloric acid and extracted 3 times with ethyl acetate (a total of 90 ml). The organic phase was washed with saturated NaCl solution, dried over Na2SO4 and filtered, and the filtrate was evaporated under reduced pressure. The product was purified by chromatography on silica gel using the eluent ethyl acetate. The yield was 266 mg of a colorless syrup (51% of theory based on the acid used).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06265611B1 |
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| 出典データセット | uspto-grants-2001_07 |
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| ORD ID | ord-752eb719072e47dc8f7bd6dcb8c146fd |
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| 出典メモ | uspto-grants-2001_07 |
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