4-tert-Butylbenzaldehyde → HCID 86603114, Verbindung

HRID 855430Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 855430
[C:1]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=O)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([N:20]([CH3:24])[CH2:21][CH2:22][NH2:23])=[CH:16][CH:15]=1.[BH4-].[Na+].[NH:27]1[C:35]2[C:30](=[CH:31][CH:32]=[CH:33][C:34]=2[C:36](O)=[O:37])[CH:29]=[CH:28]1.CCN=C=NCCCN(C)C.Cl>CO>[C:1]([C:5]1[CH:12]=[CH:11][C:8]([CH2:9][N:23]([CH2:22][CH2:21][N:20]([C:17]2[CH:16]=[CH:15][C:14]([Cl:13])=[CH:19][CH:18]=2)[CH3:24])[C:36]([C:34]2[CH:33]=[CH:32][CH:31]=[C:30]3[C:35]=2[NH:27][CH:28]=[CH:29]3)=[O:37])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]

Komponenten

7

Versuchsvorschrift

81 mg (0.5 mmol) of 4-tert-butyl benzaldehyde and 92 mg (0.5 mmol) of N-(4-chloro-phenyl)-N-methyl-ethane-1,2-diamine were dissolved in 2 ml methanol and the solution was stirred for 2 h at rt. 18.5 mg (0.5 mmol) of sodium borohydride were added in portions under nitrogen. The reaction mixture was stirred at rt for 30 min, the solvent was evaporated and the residue was suspended in 4 ml DCM. 88 mg (0.55 mol) of 1H-indole-7-carboxylic acid and 105 mg (0.55 mmol) of EDC.HCl were added and the mixture was stirred at rt over night. The product was purified by column chromatography (silica gel, diethyl ether) to yield 140 mg (59%) product as a colorless oil. MS (ISP) 474.4 (M+H)+.

Aufarbeitung

  1. stirringThe reaction mixture was stirred at rt for 30 min
  2. customthe solvent was evaporated
  3. stirringthe mixture was stirred at rt over night
  4. customThe product was purified by column chromatography (silica gel, diethyl ether)

Quellen und Nachweise

ORD-Eintrag
ord-3b3fd4fb26444835a236ffb533003970
Quelldatensatz
uspto-grants-2007_08
Patentnummer
US07259183B2

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