関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phosphoric Acid | HCID 1004 | — |
| 反応物 | Boron trifluoride etherate | HCID 8000 | — |
| 反応物 | Isobutylene | HCID 8255 | — |
| 反応物 | tert-Butyl 4-(3-aminopyridin-2-yl)piperazine-1-carboxylate | HCID 2756375 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-[3-(1,1-Dimethylethylamino)pyridyl]piperazine | HCID 11042683 | — |
反応手順
Isobutylene (10 ml) is condensed into a solution of 1-[1,1-dimethylethoxycarbonyl]-4-[3-amino-2-pyridinyl]piperazine (International Publication No. WO 88/08424, 200 mg) in methylene chloride (10 ml) at -70°. Phosphoric acid (85%, 50 μl) is added and the mixture stirred for 60 minutes. Boron trifluoride etherate (200 μl) is added dropwise and the resulting suspension is stirred 8 hours at reflux and overnight at 20°-25° allowing the isobutylene to evaporate. The suspension is diluted with water and ammonium hydroxide is added until basic to pH paper and then extracted with methylene chloride (3×). The combined extracts are dried over anhydrous potassium carbonate, filtered, and concentrated under reduced pressure to a liquid which is flash chromatographed (silica gel, 230-400 mesh), eluting with methanol/chloroform (3/20). The appropriate fractions are pooled and concentrated to give an oil. The NMR, CMR, IR, and MS (m/e) M+234 support the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05563142 |
|---|
| 出典データセット | uspto-grants-1996_10 |
|---|
| ORD ID | ord-0d5b3b596cf74a5a99b371d546b9b039 |
|---|
| 出典メモ | uspto-grants-1996_10 |
|---|