Ammonia → HCID 178519929、化合物

HRID 55491ノート

反応式

HRID 55491 の反応式
[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

  1. customThe aqueous mixture was evaporated to dryness
  2. customthe resulting residue was purified by column chromatography through silica gel
  3. washa gradient elution method
  4. 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

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