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2,6-Diethylaniline → 8-Amino-N-(2,6-diethylphenyl)-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide

HRID 81972
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 81972
C[Si](C)(C)[N-][Si](C)(C)C.[Na+].[CH2:11]([C:13]1[CH:19]=[CH:18][CH:17]=[C:16]([CH2:20][CH3:21])[C:14]=1[NH2:15])[CH3:12].[NH2:22][C:23]1[N:32]=[CH:31][C:30]2[CH2:29][CH2:28][C:27]3[C:33]([C:37](OCC)=[O:38])=[N:34][N:35]([CH3:36])[C:26]=3[C:25]=2[N:24]=1>C1COCC1>[NH2:22][C:23]1[N:32]=[CH:31][C:30]2[CH2:29][CH2:28][C:27]3[C:33]([C:37]([NH:15][C:14]4[C:16]([CH2:20][CH3:21])=[CH:17][CH:18]=[CH:19][C:13]=4[CH2:11][CH3:12])=[O:38])=[N:34][N:35]([CH3:36])[C:26]=3[C:25]=2[N:24]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 113692,6-DiethylanilineHCID 2724254Sodium bis(trimethylsilyl)amideHCID 24993827ethyl 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate

Produkt 1

HCID 670756638-Amino-N-(2,6-diethylphenyl)-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamideAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028
Tetrahydrofuran
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Sodium hexamethyldisilazide (NaHMDS) in THF (1.0 M, 11.0 mL, 11.0 mmol) was added over 30 min to a solution of 2,6-diethylaniline (1.2 mL, 8.32 mmol) and ethyl 8-amino-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate (0.760 g, 2.77 mmol) in THF (30 mL) at 0° C. The resulting brown solution was stirred at 0° C. for 10 min and allowed to warm to room temperature over a period of 30 min. After stirring at room temperature for 3 h, the reaction was quenched by the addiction of saturated acquesous NH4Cl (10 mL). The reaction was partitioned between ethyl acetate (50 mL) and water (50 mL). The acqueos layer was extracted with ethyl acetate (2×30 mL). The combined organic solution was washed with brine (50 mL), dried over Na2SO4, filtered and evaporated to dryness, the crude solid was purified by flash chromatography on silica gel (eluant: dichloromethane/methanol 95/5) to afford 0.830 g (80% yield) of the title compound.

Aufarbeitung

  1. temperatureto warm to room temperature over a period of 30 min
  2. stirringAfter stirring at room temperature for 3 h
  3. customthe reaction was quenched by the addiction of saturated acquesous NH4Cl (10 mL)
  4. customThe reaction was partitioned between ethyl acetate (50 mL) and water (50 mL)
  5. extractionThe acqueos layer was extracted with ethyl acetate (2×30 mL)
  6. washThe combined organic solution was washed with brine (50 mL)
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. customevaporated to dryness
  10. customthe crude solid was purified by flash chromatography on silica gel (eluant: dichloromethane/methanol 95/5)

Quellen und Nachweise

ORD-Eintrag
ord-597af241cbeb408ea88761810cd93bdf
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08846701B2

Notizen zur Reaktion

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