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Water → 7-(Cyclopentylamino)-2-phenyl-1H-indole-5-carboxylic acid

HRID 1466500
ノート
印刷プレビュー

反応式

HRID 1466500 の反応式
C([O:3][C:4]([C:6]1[CH:7]=[C:8]2[C:12](=[C:13]([NH:15][CH:16]3[CH2:20][CH2:19][CH2:18][CH2:17]3)[CH:14]=1)[NH:11][C:10]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[CH:9]2)=[O:5])C.O.[OH-].[Na+]>CO>[CH:16]1([NH:15][C:13]2[CH:14]=[C:6]([C:4]([OH:5])=[O:3])[CH:7]=[C:8]3[C:12]=2[NH:11][C:10]([C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)=[CH:9]3)[CH2:17][CH2:18][CH2:19][CH2:20]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 252139517-(Cyclopentyl)amino-2-phenyl-1H-indole-5-carboxylic acid ethyl ester

生成物 1

HCID 252141807-(Cyclopentylamino)-2-phenyl-1H-indole-5-carboxylic acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

7-(Cyclopentyl)amino-2-phenyl-1H-indole-5-carboxylic acid ethyl ester (5 g, 14.3 mmol) prepared in Example 28 was added to a solvent mixture of MeOH (20 mL) and water (20 mL). NaOH (1.3 g, 33.8 mmol) was added thereto, and the mixture was stirred for 4 h at room temperature. After completion of the reaction, MeOH was removed under reduced pressure, and 1N HCl was added to the residue. The resulting mixture was extracted with EtOAc, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was recrystallized from EtOAc and n-Hex to give the title compound.

後処理

  1. customwas removed under reduced pressure, and 1N HCl
  2. additionwas added to the residue
  3. extractionThe resulting mixture was extracted with EtOAc
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. customThe solvent was removed under reduced pressure
  7. customthe residue was recrystallized from EtOAc and n-Hex

出典と根拠

ORDレコード
ord-9cd329266d954f9b82459e89719cd4b9
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09000028B2

反応ノート

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