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N,N'-Dimethylethylenediamine → 6-chloro-1-(1-propyl-1H-pyrazol-4-yl)-1H-indole

HRID 522753
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HRID 522753 반응식
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][C:7](=O)[NH:8]2)=[CH:4][CH:3]=1.CNCCNC.P([O-])([O-])([O-])=O.[K+].[K+].[K+].Br[C:27]1[CH:28]=[N:29][N:30]([CH2:32][CH2:33][CH3:34])[CH:31]=1>C1(C)C=CC=CC=1.[Cu]I>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][N:8]2[C:27]2[CH:28]=[N:29][N:30]([CH2:32][CH2:33][CH3:34])[CH:31]=2)=[CH:4][CH:3]=1
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7

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HCID 8070N,N'-DimethylethylenediamineHCID 62657Potassium Phosphate, TribasicHCID 7363446-Chloro-1,3-dihydroindol-2-oneHCID 218597074-Bromo-1-propyl-1H-pyrazole2회

생성물 1

HCID 1180942196-chloro-1-(1-propyl-1H-pyrazol-4-yl)-1H-indole수율 88%

시약·촉매·용매 2

HCID 24350
Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
촉매
HCID 1140Toluene용매

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온도
140 °C

실험 절차

To a stirred solution of 6-chloro-1H-indole 1 (1.0 g, 6.62 mmol) in toluene (25 mL) under inert atmosphere were added N,N′-dimethylethylene diamine (233 mg, 2.64 mmol), potassium phosphate (3.50 g, 16.55 mmol) and 4-bromo-1-propyl-1H-pyrazole (Intermediate B; 1.23 g, 6.62 mmol) at RT and then degassed under argon for 15 min. To this, CuI (126 mg, 0.66 mmol) was added and sealed the tube. The reaction mixture was heated to 140° C. and stirred for 12 h. The reaction was monitored by TLC; after completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure to obtain the crude. This was purified by silica gel column chromatography using 10-15% EtOAc/Hexanes to afford compound 2 (1.5 g, 88%) as yellow oil. 1H NMR (500 MHz, CDCl3): δ 7.68 (s, 1H), 7.62 (s, 1H), 7.55 (d, J=10.0 Hz, 1H), 7.35 (s, 1H), 7.17 (d, J=3.5 Hz, 1H), 7.11 (d, J=10.0 Hz, 1H), 6.59 (d, J=3.5 Hz, 1H), 4.17 (t, J=7.5 Hz, 2H), 2.00-1.96 (m, 2H), 1.00 (t, J=7.5 Hz, 3H); LC-MS (ESI): 93.3%; m/z 260.2 (M+H+); (column: X Select CSH C-18, 50×3.0 mm, 3.5 μm); RT 4.04 min; 5 mM NH4OAc: ACN; 0.8 mL/min).

후처리

  1. customdegassed under argon for 15 min
  2. customsealed the tube
  3. customafter completion of the reaction
  4. filtrationthe reaction mixture was filtered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customto obtain the crude
  7. customThis was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-aec1d3a7ea5346b7b3ae19647b9a1f16
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09334261B2

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