化工社化工社 化学情報印刷レポート · 研究参考用
HRID 484512作成日:2026年10月25日
Sodium Carbonate → 3-Bromo-6-[4-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]-1-piperazinyl]pyridazine
https://huagongshe.com/reaction/484512
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 3,6-Dibromopyridazine | HCID 248852 | — |
| 反応物 | 1-[3-[4-(4,5-Dihydro-2-oxazolyl)phenoxy]propyl]piperazine | HCID 14989179 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-Bromo-6-[4-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]-1-piperazinyl]pyridazine | HCID 14989297 | 16.4% |
反応手順
A mixture of 4.1 parts of 3,6-dibromopyridazine, 4.34 parts of 1-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]piperazine, 6.4 parts of sodium carbonate and 1878 parts of N,N-dimethylformamide was stirred overnight at 65° C. The reaction mixture was poured into ice water and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol 98.5:1.5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2-propanol. The product was filtered off and dried, yielding 1.1 parts (16.4%) of 3-bromo-6-[4-[3-[4(4,5-dihydro-2-oxazolyl)phenoxy]propyl]-1-piperazinyl]pyridazine; mp. 169.1° C. (comp. 75).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05231184 |
|---|
| 出典データセット | uspto-grants-1993_07 |
|---|
| ORD ID | ord-88af42f5eb6e40948beb22d5d10e5c98 |
|---|
| 出典メモ | uspto-grants-1993_07 |
|---|