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t-butyl 4-(1-benzenesulfonyl-1H-indol-4-yl)piperazine-1-carboxylate → 1-(Phenylsulfonyl)-4-(1-piperazinyl)-1h-indole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | t-butyl 4-(1-benzenesulfonyl-1H-indol-4-yl)piperazine-1-carboxylate | HCID 22015366 | — |
| 溶媒 | Trifluoroacetic acid | HCID 6422 | — |
| 生成物 | 1-(Phenylsulfonyl)-4-(1-piperazinyl)-1h-indole | HCID 10154392 | — |
反応手順
A solution of 125 mg (0.28 mmole) 4-(1-benzenesulfonyl-1H-indol-4-yl)-piperazine-1-carboxylic acid tert-butyl ester in 2 mL trifluoroacetic acid was stored at room temperature for 10 minutes. The solution was concentrated under reduced pressure and the residue was partitioned between 3 mL 10% sodium carbonate and 20 mL ethyl acetate. The organic phase was washed with 5 mL water, dried (magnesium sulfate) and concentrated. 1-Benzenesulfonyl-4-piperazin-1-yl-1H-indole (5) was isolated as the hydrochloride salt from ethyl acetate-ethyl ether, 73 mg, M+H=342; m.p.294-295° 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-739071936fc645228785cdc460a703e5 |
| 出典メモ | uspto-grants-2004_09 |