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Dichloromethane → 3-[4-[4-(3-Chlorophenyl)-1-piperazinyl]butyl]-3-azabicyclo[3.2.1]octane-2,4-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | O-Xylene | HCID 7237 | — |
| 反応物 | 1,3-Cyclopentanedicarboxylic anhydride | HCID 239799 | — |
| 反応物 | 4-[4-(3-Chlorophenyl)piperazin-1-yl]butan-1-amine | HCID 12840704 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 3-[4-[4-(3-Chlorophenyl)-1-piperazinyl]butyl]-3-azabicyclo[3.2.1]octane-2,4-dione | HCID 14156369 | — |
反応手順
1,3-Cyclopentane dicarboxylic anhydride (2.2 g., 15 mmole) and 4.0 g. (15 mmole) of 1-(4-aminobutyl)-4-(3-chlorophenyl)piperazine were combined in 300 ml. of methylene chloride and stirred for 30 minutes at room temperature. The solvent was replaced with xylene and the mixture was refluxed for 48 hours with water removal via a Dean-Stark trap. The solvent was removed in vacuum and the residue filtered through 75 g. of silica gel with 2% ethanol/chloroform as eluent. The product was concentrated in vacuum and crystallized from 50 ml. of isopropanol with addition of 4N isopropanolic HCl. Recrystallization from ethanol gave 1.6 g. of the title compound as the hydrochloride, quarter hydrate; m.p. 199°-202° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04748240 |
| 出典データセット | uspto-grants-1988_05 |
| ORD ID | ord-0414f49d39d6428e8394f535d7f0ce73 |
| 出典メモ | uspto-grants-1988_05 |