関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 4-(Bromoacetyl)pyridine hydrobromide | HCID 2776239 | — |
| 反応物 | HCID 178479085 | HCID 178479085 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-(pyridin-4-yl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole | HCID 19879236 | — |
反応手順
A stirred suspension of 10 g (35.6 mmoles) of 4-(bromoacetyl)-pyridine hydrobromide and 12.9 g (107 mmoles) of 2-imino-pyrrolidine hydrochloride in 100 ml of dry dimethylformamide was treated with 18.9 g (178 mmoles) of anhydrous sodium carbonate. This suspension was heated at 80° C. overnight in an oil bath. The solvent was removed in vacuo, the residue dissolved in water and extracted with chloroform. The organic layer was washed three times with water, dried over anhydrous potassium carbonate and stripped in vacuo. The residue was chromatographed on silica and eluted with 10-15% methanol in methylene chloride acetone (85:15). This fraction was stripped in vacuo and the solid residue recrystallized twice from ethyl acetate to afford the desired titled compound, mp 140°-141° C., 1HNMR (250 MHz, CDCl3) δ 8.62 (2H,d), 7.60(2H,d), 7.34(1H,s), 4.04(2H,t), 2.95 (2H,t), 2.64(2H,q).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05145858 |
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| 出典データセット | uspto-grants-1992_09 |
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| ORD ID | ord-57ee2631cd574db8af1c8fd9ab36138d |
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| 出典メモ | uspto-grants-1992_09 |
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