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Water → N-[2-[2-[(1,1-dimethylethyl)amino]ethoxy]phenyl]-1H-indol-4-carboxamide

HRID 1768976
ノート
印刷プレビュー

反応式

HRID 1768976 の反応式
Cl[CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[NH:11][C:12]([C:14]1[C:15]2[CH:16]=[CH:17][NH:18][C:19]=2[CH:20]=[CH:21][CH:22]=1)=[O:13].O.[OH-].[Na+].C(=O)([O-])[O-].[K+].[K+].[C:32]([NH2:36])([CH3:35])([CH3:34])[CH3:33]>C(O)C.C(OCC)(=O)C>[CH3:33][C:32]([NH:36][CH2:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[NH:11][C:12]([C:14]1[C:15]2[CH:16]=[CH:17][NH:18][C:19]=2[CH:20]=[CH:21][CH:22]=1)=[O:13])([CH3:35])[CH3:34]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 962WaterHCID 6385Tert-ButylamineHCID 11430Potassium CarbonateHCID 14798Sodium HydroxideHCID 13787419N-[2-(2-chloroethoxy)phenyl]-1H-indol-4-carboxamide

生成物 1

HCID 3086996N-[2-[2-[(1,1-dimethylethyl)amino]ethoxy]phenyl]-1H-indol-4-carboxamide

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 8857Ethyl Acetate溶媒

実験手順

With stirring at a pressure of 2 bars, a solution of 2.3 g of the product from Step A in 40 ml of ethanol and 37.5 ml of tert-butyl-amine was heated at 120° C. for 24 hours. After dilution with 400 ml of water and 400 ml of ethyl acetate, the solution was alkalized with sodium hydroxide and saturated with potassium carbonate. The mixture was extracted with ethyl acetate and the crystals obtained were triturated with ether to obtain 2.3 g of N-[2-[2-[(1,1-dimethylethyl)amino]ethoxy]phenyl]-1H-indol-4-carboxamide melting at ≃148° C.

後処理

  1. extractionThe mixture was extracted with ethyl acetate
  2. customthe crystals obtained
  3. customwere triturated with ether

出典と根拠

ORDレコード
ord-4c8ee46290584f3a836b9260212258b5
出典データセット
uspto-grants-1995_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05380722

反応ノート

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