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5-Nitro-3-isoquinolinecarboxylic acid → 5-Aminoisoquinoline-3-carboxylic acid

HRID 1902550
ノート
印刷プレビュー

反応式

HRID 1902550 の反応式
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[C:7]([C:14]([OH:16])=[O:15])[N:8]=[CH:9]2)([O-])=O>CO.[Pd]>[NH2:1][C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[C:7]([C:14]([OH:16])=[O:15])[N:8]=[CH:9]2
参加物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 193906095-Nitro-3-isoquinolinecarboxylic acid

生成物 1

HCID 205156525-Aminoisoquinoline-3-carboxylic acid収率 92.2%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

5-Nitroisoquinoline-3-carboxylic acid (44 g) is dissolved in methanol (3 liters), and a catalyst consisting of palladium-on-carbon (3/97 by weight; 15 g) is added. The mixture is hydrogenated at atmospheric pressure, at a temperature between 20° and 25° C. After stirring for 5 hours, the volume of hydrogen absorbed is 13.9 liters. The mixture is filtered through diatomaceous silica and the filtrate is concentrated to dryness under reduced pressure (20 mm Hg; 2.7 kPa) at 60° C. to yield 5-aminoisoquinoline-3-carboxylic acid (35 g).

後処理

  1. additionis added
  2. customis hydrogenated at atmospheric pressure, at a temperature between 20° and 25° C
  3. customthe volume of hydrogen absorbed
  4. filtrationThe mixture is filtered through diatomaceous silica
  5. concentrationthe filtrate is concentrated to dryness under reduced pressure (20 mm Hg; 2.7 kPa) at 60° C.

出典と根拠

ORDレコード
ord-f408aa0ee97740cc8926906d0cd84de3
出典データセット
uspto-grants-1982_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04363909

反応ノート

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