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O-Xylene → 3-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-8,8-dimethyl-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 | O-Xylene | HCID 7237 | — |
| 反応物 | 4-(2-Pyrimidinyl)-1-piperazinebutanamine | HCID 12840705 | — |
| 反応物 | 8,8-Dimethyl-3-oxabicyclo(3.2.1)octane-2,4-dione | HCID 19797203 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 3-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-8,8-dimethyl-3-azabicyclo[3.2.1]octane-2,4-dione | HCID 14097164 | — |
反応手順
2,2-Dimethylcyclopentane-1,3-dicarboxylic anhydride (1.68 g., 10 mmole) and 1-(4-aminobutyl)-4-(2-pyrimidinyl)piperazine (2.55 g., 11 mmole) were combined in 500 ml. of xylene and refluxed for 48 hours with water removal via a Dean-Stark trap. The solvent was removed in vacuo and the residue column chromatographed on 100 g. of silica gel using a gradient elution from straight chloroform to 5% ethanol/chloroform. Concentration of the product in vacuum and recrystallization from isopropanol with addition of 4N isopropanolic HCl and acetone gave 600 mg. of the title compound as the dihydrochloride, monohydrate; m.p. 227°-229° C. (d).
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-8ddbe2487e454406bb2cccb7cc2b861b |
| 出典メモ | uspto-grants-1988_05 |