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1,1'-Carbonyldiimidazole → NGB 2904 hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 反応物 | 9H-fluorene-2-carboxylic acid | HCID 348591 | — |
| 反応物 | 1-Piperazinebutanamine, 4-(2,3-dichlorophenyl)- | HCID 11098669 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | NGB 2904 hydrochloride | HCID 19366304 | 139.4% |
反応手順
A mixture of 9H-fluorene-2-carboxylic acid (100 mg, 0.48 mmol) and 1.1'-carbonyldiimidazole (80 mg, 0.5 mmol) in 10 mL of anhydrous tetrahydrofuran was stirred for 8 hours. A solution of 4-[4-(2,3-dichlorophenyl)-1-piperazinyl]-1-aminobutane (150 mg, 0.5 mmol) in 1 mL of tetrahydrofuran was added and the resulting mixture was stirred for 30 minutes. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with aqueous Na2CO3 solution, dried (Na2SO4) and concentrated in vacuo to give the title compound (185 mg, 78%). Hydrochloride salt was prepared by treating the free base with a solution of hydrogen chloride in ethyl acetate (mp 262-4° C.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06015900 |
| 出典データセット | uspto-grants-2000_01 |
| ORD ID | ord-2492c9d164984b47b86e64cff738f390 |
| 出典メモ | uspto-grants-2000_01 |