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1-Piperazinecarboxylic acid, ethyl ester → Ethyl 4-[(8-hydroxyquinolin-5-yl)methyl]piperazine-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Piperazinecarboxylic acid, ethyl ester | HCID 8431 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 8-Quinolinol, 5-(chloromethyl)-, hydrochloride (1:1) | HCID 12269596 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Ethyl 4-[(8-hydroxyquinolin-5-yl)methyl]piperazine-1-carboxylate | HCID 1090305 | 42.9% |
反応手順
N-Ethoxycarbonylpiperazine (1.5 ml, 10.2 mmol) was added to a mixture of 5-chloromethyl-8-hydroxyquinoline hydrochloride (2.36 g, 10.2 mmol) and diisopropylethylamine (3.6 ml, 20.6 mmol) in CHCl3 (50 ml) at 5° C. The mixture was stirred for 24 h at room temperature. CHCl3 (100 ml) was then added and the solution was washed with 5% NaHCO3 (3×50 ml) and brine (2×50 ml) and then dried over Na2SO4. The solution was filtered and evaporated to dryness. The residue was crystallized from a mixture of benzene hexane and gave 1.38 g (42%) of the title product. M.p. −96° C. TLC (CHCl3-MeOH-NH3 9:1:0.1) Rf=0.6; TLC (CHCl3-MeOH-Me3 9:0.5:0.05) Rf−0.4.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06855711B1 |
| 出典データセット | uspto-grants-2005_02 |
| ORD ID | ord-42f95f73faf44ca99a56964d76d6bf47 |
| 出典メモ | uspto-grants-2005_02 |