Ammonium formate → 3-(1H-indol-2-yl)-1H-indazol-5-ol

HRID 1726048ノート

反応式

HRID 1726048 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([O:19]C3C=CC=CC=3)[CH:17]=2)[NH:12][N:11]=1.C([O-])=O.[NH4+]>C(O)C.[Pd]>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([OH:19])[CH:17]=2)[NH:12][N:11]=1

参加物

5

反応物 2

HCID 2723923Ammonium formateHCID 1363420653-(1H-indol-2-yl)-5-phenoxy-1H-indazole

生成物 1

HCID 1360559793-(1H-indol-2-yl)-1H-indazol-5-ol収率 89.4%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

A solution of 2.54 g of 3-(1H-indol-2-yl)-5-phenoxy-1H-indazole, of 2.83 g of ammonium formate and 2.54 g of palladium-on-charcoal at 10% in 150 ml of ethanol is refluxed for one hour. The catalyst is filtered through paper and rinsed with ethanol. The filtrate is concentrated to dryness to obtain 1.74 g of 3-(1H-indol-2-yl)-1H-indazol-5-ol.

後処理

  1. filtrationThe catalyst is filtered through paper
  2. washrinsed with ethanol
  3. concentrationThe filtrate is concentrated to dryness

出典と根拠

ORDレコード
ord-54d6543ecafe4281aa0970c7f41132e1
出典データセット
uspto-grants-2009_02
特許番号
US07491710B2

反応ノート

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