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Sodium hydride → N1-methyl-5-(2-amino-5-cyano-4-pyridyl)oxy-1H-1-indolecarboxamide

HRID 2376917
ノート
印刷プレビュー

反応式

HRID 2376917 の反応式
[NH2:1][C:2]1[CH:9]=[C:8]([O:10][C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[NH:16][CH:15]=[CH:14]3)[C:5]([C:6]#[N:7])=[CH:4][N:3]=1.[H-].[Na+].[CH2:22]([NH:25][C:26](=O)[O:27]C1C=CC=CC=1)CC.[Cl-].[NH4+]>CN(C)C=O>[CH3:22][NH:25][C:26]([N:16]1[C:17]2[C:13](=[CH:12][C:11]([O:10][C:8]3[C:5]([C:6]#[N:7])=[CH:4][N:3]=[C:2]([NH2:1])[CH:9]=3)=[CH:19][CH:18]=2)[CH:14]=[CH:15]1)=[O:27]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 11252326Carbamic acid, propyl-, phenyl esterHCID 219493966-Amino-4-(1H-5-indolyloxy)nicotinonitrile

生成物 1

HCID 21949164N1-methyl-5-(2-amino-5-cyano-4-pyridyl)oxy-1H-1-indolecarboxamide収率 22%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

6-Amino-4-(1H-5-indolyloxy)nicotinonitrile (63 mg, 0.252 mmol) was dissolved in N,N-dimethylformamide (1 ml); and sodium hydride (60% in oil, 11.6 mg, 0.29 mmol) was gradually added thereto while stirring at room temperature. After the reaction mixture was stirred for 30 minutes, phenyl N-propylcarbamate (49.5 mg, 0.277 mmol) was added thereto; and the reaction mixture was stirred for 3 hours. A saturated aqueous solution of ammonium chloride was added thereto; this was subjected to extraction with ethyl acetate, and dried over anhydrous sodium sulfate. This solution was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Fuji Silysia NH, ethyl acetate-methanol) to yield the title compound (12 mg) and N1-methyl-5-(2-amino-5-cyano-4-pyridyl)oxy-1H-1-indolecarboxamide (17 mg).

後処理

  1. stirringAfter the reaction mixture was stirred for 30 minutes
  2. stirringand the reaction mixture was stirred for 3 hours
  3. extractionthis was subjected to extraction with ethyl acetate
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationThis solution was concentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (Fuji Silysia NH, ethyl acetate-methanol)

出典と根拠

ORDレコード
ord-38df84226070485bba5df3b9f7697357
出典データセット
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07468380B2

反応ノート

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