Ammonia → HCID 178519929、化合物
反応式
[C:1]([OH:5])(=O)[CH2:2]O.[Cl:6][C:7]1[N:12]=[C:11]([NH2:13])[C:10]([NH2:14])=[CH:9][CH:8]=1.Cl.N>>[Cl:6][C:7]1[N:12]=[C:11]2[NH:13][C:2]([CH2:1][OH:5])=[N:14][C:10]2=[CH:9][CH:8]=1参加物
5
反応条件
- 温度
- 150 °C
実験手順
6.60 g of glycolic acid were added to 5.00 g of 6-chloro-2,3-diaminopyridine (prepared as described in Preparation 42), and the resulting mixture was stirred at 150° C. for 4 hours. At the end of this time, the reaction mixture was treated with 3N aqueous hydrochloric acid and subsequently made alkaline by the addition of aqueous ammonia. The aqueous mixture was evaporated to dryness, and the resulting residue was purified by column chromatography through silica gel, using a gradient elution method, with mixtures of ethyl acetate and methanol in ratios ranging from 1:0 to 10:1 by volume as the eluent. The product was then crystallized by trituration with ethyl acetate, to give 5.33 g of the title compound, melting at 224°-226° C.
後処理
- customThe aqueous mixture was evaporated to dryness
- customthe resulting residue was purified by column chromatography through silica gel
- washa gradient elution method
- customThe product was then crystallized by trituration with ethyl acetate
出典と根拠
- ORDレコード
- ord-635b4ec7e35d4c8e9528b9b32b08a17f
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05624935
反応ノート
読み込み中…