化工社化工社 化学情報印刷レポート · 研究参考用
Tetrabutylammonium Fluoride → 4-(4-Benzyl-piperazin-1-yl)-1H-indole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 反応物 | 1-triisopropylsilanyl-4-(4-benzyl-piperazin-1-yl)-1H-indole | HCID 22671261 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-(4-Benzyl-piperazin-1-yl)-1H-indole | HCID 2728532 | — |
反応手順
To a solution of 1.2 gram (2.68 mmole) 1-triisopropylsilanyl-4-(4-benzyl-piperazin-1-yl)-1H-indole in 20 mL tetrahydrofuran was added 3 mL (3 mmole) 1.0 M tetrabutylammonium fluoride in tetrahydrofuran. After 2 hours the solution was concentrated under reduced pressure and the residue was partitioned between 25 mL ethyl ether and 10 mL 10% sodium carbonate. The organic phase was washed with 3×10 mL water, dried (magnesium sulfate), and concentrated. 4-(4-Benzyl-piperazin-1-yl)-1H-indole was isolated as the white hydrochloride salt from ethyl ether, 604 mg, m.p. 233-234° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06790848B2 |
| 出典データセット | uspto-grants-2004_09 |
| ORD ID | ord-26dcf6bbf05a427292e269124172fdfc |
| 出典メモ | uspto-grants-2004_09 |