関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Methyl-2-butanol | HCID 6405 | — |
| 反応物 | Chloride 2-chloropyridinium 1-oxide | HCID 88478 | — |
| 反応物 | N-BOC-ethylenediamine | HCID 187201 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 178453672 | HCID 178453672 | 89.3% |
反応手順
A mixture of mono-Boc-1,2-ethylenediamine (5.83 g, 36.39 mmole), 2-chloropyridine-N-oxide hydrochloride (7.25 g, 43.67 mmole), NaHCO3 (15.29 g, 182 mmole), and tert-amyl alcohol (36 mL) was heated at reflux. After 47 hr, the dark brown mixture was cooled, diluted with CH2Cl2 (100 mL), and suction filtered to remove insoluble materials. The filtrate was concentrated and reconcentrated from toluene. Silica gel chromatography (10% MeOH/CHCl3) gave impure title compound (8.23 g, 89%) as a yellow solid which was used without further purification: TLC (10% MeOH/CHCl3) Rf 0.42; 1H NMR (250, CDCl3) δ 8.16 (dd, J=6.5, 1.3 Hz, 1H), 7.05-7.30 (m, 2H), 6.68 (br d, J=8.6 Hz, 1H), 6.50-6.65 (m, 1H), 5.70-5.95 (m, 1H), 3.25-3.60 (m, 4H), 1.44 (s, 9H); MS (ES) m/e 254 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06191304B1 |
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| 出典データセット | uspto-grants-2001_02 |
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| ORD ID | ord-fdde1fe236b64b578564db116858de23 |
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| 出典メモ | uspto-grants-2001_02 |
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