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Triethylamine → 5-Aminoindole

HRID 1419166
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HRID 1419166 반응식
CC1[N:3]([C:8]2[CH:9]=[C:10]3[C:14](=[CH:15][CH:16]=2)[NH:13][CH:12]=[CH:11]3)C(C)=CC=1.Cl.NO.C(N(CC)CC)C.[OH-].[Na+]>CC(O)C.O>[NH2:3][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[NH:13][CH:12]=[CH:11]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 100818535-(2,5-dimethyl-1H-pyrrol-1-yl)-1H-indole

생성물 1

HCID 788675-Aminoindole

시약·촉매·용매 2

HCID 962Water용매
HCID 3776
Isopropanol
용매

실험 절차

A mixture of the 5-(2,5-dimethyl-1H-pyrrol-1-yl)-1H-indole (10.00 mmol), hydroxylamine hydrochloride (6.95 g, 100 mmol, 10 eq), and triethylamine (6.97 mL, 50.0 mmol, 5 eq) in 2-propanol (35 mL) and water (5 mL) was heated at reflux under nitrogen for a time depending on the substrate. The resulting reaction mixture was cooled, solid sodium hydroxide (4.00 g, 100 mmol, 10 eq) was added, and the resulting reaction mixture was stirred at room temperature under nitrogen for 24 hours. The reaction mixture was then filtered through Celite®, and the filtrate was evaporated under reduced pressure. The residue was column chromatographed using silica gel (approximately 100 g) and eluting with an appropriate solvent system to afford the appropriate 5amino-1H-indole.

후처리

  1. temperaturewas heated
  2. temperatureat reflux under nitrogen for a time
  3. customThe resulting reaction mixture
  4. temperaturewas cooled
  5. customthe resulting reaction mixture
  6. filtrationThe reaction mixture was then filtered through Celite®
  7. customthe filtrate was evaporated under reduced pressure
  8. customchromatographed
  9. washeluting with an appropriate solvent system

출처 및 근거

ORD 기록
ord-f47359dd4050490e9f6f265bbea4c541
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05886008

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