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Potassium Carbonate → (1-Benzyl-4-piperidyl)methyl-3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-Bromo-1-propanol | HCID 12308 | — |
| 反応物 | Chlorosuccinimide | HCID 31398 | — |
| 反応物 | (1-Benzyl-4-piperidyl)methyl indole-3-carboxylate | HCID 19599412 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | (1-Benzyl-4-piperidyl)methyl-3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxylate | HCID 44211270 | — |
反応手順
(1-Benzyl-4-piperidyl)methyl indole-3-carboxylate was treated initially with N-chlorosuccinimide (1.5 equivalents) for 2 h, then with 3-bromo-1-propanol (2 equivalents) for 16 h, followed by anhydrous potassium carbonate in acetone, using the method described in Example 1b. The crude product was purified by chromatography on silica gel eluting with chloroform/ethanol (19:1) to afford the title compound (E15) as a beige solid following recrystallisation from chloroform/ether (47%) mp 158°-160° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05852014 |
| 出典データセット | uspto-grants-1998_12 |
| ORD ID | ord-0aaf56a8cf2c47a592c4f2fd8eb60abc |
| 出典メモ | uspto-grants-1998_12 |