Hydrochloric Acid → HCID 20135762、化合物
反応式
[CH2:1]([N:3]([CH2:23][CH3:24])[CH2:4][CH2:5][CH2:6][NH:7][C:8]1[C:16]2[C:11](=[C:12]([N+:20]([O-])=O)[CH:13]=[C:14]([N+:17]([O-])=O)[CH:15]=2)[NH:10][N:9]=1)[CH3:2].CO.O.Cl>[Fe].C(Cl)(Cl)Cl>[CH2:23]([N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][CH2:6][NH:7][C:8]1[C:16]2[C:11](=[C:12]([NH2:20])[CH:13]=[C:14]([NH2:17])[CH:15]=2)[NH:10][N:9]=1)[CH3:24]参加物
反応条件
- 温度
- 70 °C
実験手順
A mixture consisting of 9.0 g of the 3-(3-diethylaminopropylamino)-5,7-dinitroindazole, 18 g of iron powder, 60 ml of methyl alcohol, 30 ml of water and 3 ml of hydrochloric acid was stirred for 1.5 hours at 70° C. After cooling, the mixture was filtered, and the pH of the filtrate was adjusted to 11 with an aqueous potassium carbonate solution. The filtrate was extracted three times with 50 ml of ethyl acetate. The ethyl acetate layer was washed with water and dried over anhydrous sodium sulfate. Then, ethyl acetate was removed under reduced pressure. The residue thus obtained was subjected to an alumina-column chromatography(alumina: 200 g) using chloroform as the developing solvent to give 1.67 g of 3-(3-diethylaminopropylamino)-5,7-diaminoindazole having the following analytical values in a yield of 22%.
後処理
- temperatureAfter cooling
- filtrationthe mixture was filtered
- extractionThe filtrate was extracted three times with 50 ml of ethyl acetate
- washThe ethyl acetate layer was washed with water
- dry with materialdried over anhydrous sodium sulfate
- customThen, ethyl acetate was removed under reduced pressure
- customThe residue thus obtained
出典と根拠
- ORDレコード
- ord-24ad1db860ad4ff0953e39622fb2551d
- 出典データセット
- uspto-grants-1988_06
- 特許番号
- US04751302
反応ノート
読み込み中…