関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexachloroethane | HCID 6214 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | 3-(2-Butynyl)-4-chloro-3H-imidazo[4,5-c]pyridine | HCID 23070729 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-(2-Butynyl)-2,4-dichloro-3H-imidazo[4,5-c]pyridine | HCID 23070980 | 21% |
反応手順
2.22 ml of a tetrahydrofuran solution of lithium diisopropylamide was added dropwise to a 5 ml tetrahydrofuran solution of 490 mg of 3-(2-butynyl)-4-chloro-3H-imidazo[4,5-c]pyridine in a dry ice-methanol bath, and the mixture was stirred below −66° C. for 20 minutes. The resulting reaction mixture was added dropwise to a 2 ml tetrahydrofuran solution of 1.13 g of hexachloroethane while the temperature of the mixture was controlled to be −63° C. or lower. The mixture was stirred for one hour and 40 minutes in the same bath, and then a saturated aqueous ammonium chloride solution was added thereto. The resulting mixture was extracted twice with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate, then filtered. The filtrate was concentrated under reduced pressure. Then, the resulting residue was purified by silica gel column chromatography. Thus, 120 mg of brown oily material was obtained from the fraction eluted with hexane-ethyl acetate (2:1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07772226B2 |
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| 出典データセット | uspto-grants-2010_08 |
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| ORD ID | ord-8adadceae381408d99ea7a971222e9dd |
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| 出典メモ | uspto-grants-2010_08 |
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