関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Trichloroisocyanuric Acid | HCID 6909 | — |
| 反応物 | Isopropylethanediol | HCID 7996 | — |
| 反応物 | 5-Aminoimidazole-4-carboxamide hydrochloride | HCID 66146 | — |
| 触媒 | Tempo | HCID 2724126 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-[(2-isopropoxyethyl)amino]-1H-imidazole-5-carboxamide | HCID 67157558 | 38.3% |
反応手順
Trichlorocyanuric acid (1.23 g, 5.29 mmol) was added to a solution of 2-isopropoxyethanol (0.50 g, 4.80 mmol) in CH2Cl2 (3 mL). The reaction mixture was cooled to 0° C. and TEMPO (0.015 g, 0.09 mmol) was carefully added in small portions. The mixture was stirred at r.t. for 20 minutes and then filtrated through Celite and washed with CH2Cl2. The filtrate was kept cold, 0° C., during the filtration. The obtained aldehyde solution was added to a stirred mixture of 4-amino-1H-imidazole-5-carboxamide hydrochloride (0.78 g, 4.80 mmol), which was obtained from Example 3(b), at 0° C. in MeOH (5 mL). The mixture was stirred for 20 minutes, then NaCNBH4 (0.30 g, 4.80 mmol) was added. After stirring at r.t for 5 h the mixture was concentrated and purified by flash chromatography (CH2Cl2/methanol gradient; 0 to 5% methanol), to yield the title compound (0.39 g, 38%) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07943625B2 |
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| 出典データセット | uspto-grants-2011_05 |
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| ORD ID | ord-6673139033054c94a3ee28934054b163 |
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| 出典メモ | uspto-grants-2011_05 |
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