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Cyclopropylamine → 7-Hydroxyindole

HRID 439395
ノート
印刷プレビュー

反応式

HRID 439395 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5]C=CC=2)[C:3](=[O:10])[CH2:2]1.[CH:11]1(N)[CH2:13][CH2:12]1>C1(C)C=CC=CC=1.[Ti](Cl)(Cl)(Cl)Cl>[NH:1]1[C:2]2[C:13](=[CH:12][CH:5]=[CH:4][C:3]=2[OH:10])[CH:11]=[CH:9]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 69828CyclopropylamineHCID 2309151,2-dihydro-3H-indol-3-one

生成物 1

HCID 27376517-Hydroxyindole

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒HCID 1140Toluene溶媒2 回

反応条件

温度
-10 °C

実験手順

7-Chloroacetyloxy-1,4-dihydro-4-methylcyclopent b!indol-3(2H)-one (15.0 g) and cyclopropylamine (9.6 g) were dissolved in 300 ml toluene and cooled to -10° C. Titanium tetrachloride (6.3 g) dissolved in 50 ml toluene was added slowly to the first solution. The reaction mixture was allowed to come up to room temperature and stirred overnight. The next day another 1.5 equivalents of the amine (4.6 g) was added to the reaction mixture and the mixture was stirred for one hour. The reaction mixture was filtered through a pad of silica gel, eluting with 3:1 hexane/ethyl acetate, giving a yellow oil after removal of solvents. 3-Cyclopropylamino-4-methyl-1,2,3,4-tetrahydrocyclopent b!-indol-7-ol was isolated as a light yellow solid (3.3 g) after flash chromatography and recrystallization from ethyl acetate.

後処理

  1. additionwas added slowly to the first solution
  2. customto come up to room temperature
  3. stirringthe mixture was stirred for one hour
  4. filtrationThe reaction mixture was filtered through a pad of silica gel
  5. washeluting with 3:1 hexane/ethyl acetate
  6. customgiving a yellow oil
  7. customafter removal of solvents

出典と根拠

ORDレコード
ord-752619c4d85e4a9cad4738d3192ff18b
出典データセット
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05514700

反応ノート

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