化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1444749作成日:2026年10月24日
6-Phenoxynicotinaldehyde → 2-phenoxy-5-((2-(pyridin-3-yl)-5,6-dihydropyridin-3(4H)-ylidene)methyl)pyridine dihydrochloride
https://huagongshe.com/ja/reaction/1444749
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 6-Phenoxynicotinaldehyde | HCID 2776500 | — |
| 反応物 | 3-(5-Ammoniopentanoyl)pyridinium chloride | HCID 67337657 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 2-phenoxy-5-((2-(pyridin-3-yl)-5,6-dihydropyridin-3(4H)-ylidene)methyl)pyridine dihydrochloride | HCID 67337936 | 147.2% |
反応手順
3-(5-Ammoniopentanoyl)pyridinium chloride (101 mg, 0.40 mmol) and 6-phenoxynicotinaldehyde (120 mg, 0.60 mmol) were combined in a reaction vessel and treated with isopropanol (15 mL). The reaction vessel was sealed and the reaction was heated to 80° C. with stirring overnight. The reaction was then cooled to room temperature. The precipitate that formed was recovered by vacuum filtration and washed with a 20% solution of isopropanol in hexane and then with ether. The recovered solid was then dried under vacuum giving 122 mg (73%) of a pale yellow solid. LC-MS: RT=5.08 min, [M+H]+=342.1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07662965B2 |
|---|
| 出典データセット | uspto-grants-2010_02 |
|---|
| ORD ID | ord-ae0f567c7dfb4e0f9b94302d12f9c479 |
|---|
| 出典メモ | uspto-grants-2010_02 |
|---|