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5-Nitro-6-(2-methoxy-4-benzyloxy-benzoylamino)-2-pyridone → HCID 178493420、化合物

HRID 35202
ノート
印刷プレビュー

反応式

HRID 35202 の反応式
[N+:1]([C:4]1[CH:5]=[CH:6][C:7](=[O:29])[NH:8][C:9]=1[NH:10][C:11](=O)[C:12]1[CH:17]=[CH:16][C:15]([O:18]CC2C=CC=CC=2)=[CH:14][C:13]=1[O:26][CH3:27])([O-])=O>C(O)(=O)C.[Pd]>[CH3:27][O:26][C:13]1[CH:14]=[C:15]([OH:18])[CH:16]=[CH:17][C:12]=1[C:11]1[N:10]=[C:9]2[NH:8][C:7](=[O:29])[CH2:6][CH:5]=[C:4]2[N:1]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 212958065-Nitro-6-(2-methoxy-4-benzyloxy-benzoylamino)-2-pyridone

生成物 1

HCID 178493420HCID 178493420、化合物

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 176Acetic Acid溶媒

反応条件

温度
100 °C

実験手順

3.95 g of 5-nitro-6-(2-methoxy-4-benzyloxy-benzoylamino)-2-pyridone were hydrogenated in 350 ml of glacial acetic acid after the addition of 1 g of 10% palladium-on-charcoal for 1.7 hours at 80° C. under a pressure of 5 bar. The reaction mixture was then stirred at 100° C. for 1.3 hours. The catalyst was filtered off, and the filtrate was allowed to cool. The product which precipitated was washed with ether. By evaporating the filtrate and adding ether, further fractions were obtained. Yield: 2.3 g (60% of theory). Melting point: over 270° C.

後処理

  1. filtrationThe catalyst was filtered off
  2. temperatureto cool
  3. customThe product which precipitated
  4. washwas washed with ether
  5. customBy evaporating the filtrate
  6. additionadding ether
  7. customfurther fractions were obtained
  8. customover 270° C.

出典と根拠

ORDレコード
ord-b5abdcdb5c4d4ab6ad43c01a3940bcc1
出典データセット
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04766130

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート