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1(2H)-Phthalazinone → 4-[2-[1-Oxo-1,2-dihydrophthalazin-2-yl]ethoxy]benzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1(2H)-Phthalazinone | HCID 8394 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-(2-Bromoethoxy)Benzaldehyde | HCID 262706 | — |
| 生成物 | 4-[2-[1-Oxo-1,2-dihydrophthalazin-2-yl]ethoxy]benzaldehyde | HCID 11140939 | 44% |
反応手順
##STR31## The title compound (700 mg, 44%) was prepared from 1(2H)-phthalazinone (800 mg, 5.48 mmol) (Ref: Chemistry of Heterocyclic Compounds; Condensed Pyridazines including Cinnolines and Phthalazines, edited by R. N. Castle; John Wiley and Sons, 27, (1973) 375-441), 4-[2-bromoethoxy]benzaldehyde (1.25 g, 5.48 mmol) and K2CO3 (1.5 g, 10.96 mmol) by a similar procedure to that described in preparation 2, mp: 104-106° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06011036 |
| 出典データセット | uspto-grants-2000_01 |
| ORD ID | ord-f5fcecb74d2c44a29148c8677187d255 |
| 出典メモ | uspto-grants-2000_01 |