Tetrahydrofuran → Ethyl 8-benzyl-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate

HRID 875086Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 875086
[Br-].[CH2:2]([Zn+])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C1COCC1.[CH3:15][N:16]1[C:28]2[C:27]3[N:26]=[C:25](SC)[N:24]=[CH:23][C:22]=3[CH2:21][CH2:20][C:19]=2[C:18]([C:31]([O:33][CH2:34][CH3:35])=[O:32])=[N:17]1.C(=O)(O)[O-].[Na+]>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C(OCC)(=O)C>[CH2:2]([C:25]1[N:24]=[CH:23][C:22]2[CH2:21][CH2:20][C:19]3[C:18]([C:31]([O:33][CH2:34][CH3:35])=[O:32])=[N:17][N:16]([CH3:15])[C:28]=3[C:27]=2[N:26]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Komponenten

7

Edukt 4

HCID 8028TetrahydrofuranHCID 516892Sodium BicarbonateHCID 45141606Ethyl 1-methyl-8-(methylthio)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylateHCID 178419772HCID 178419772, Verbindung

Produkt 1

HCID 57444089Ethyl 8-benzyl-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178418397HCID 178418397, VerbindungKatalysatorHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

Under a nitrogen atmosphere, a 0.5 M solution of benzylzinc bromide in THF (3.11 mL, 1.556 mmol) was added to a mixture of ethyl 1-methyl-8-(methylthio)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate (237 mg, 0.778 mmol) and Pd(PPh3)4 (9 mg, 0.0078 mmol, 1%). After 20 hours of heating at 60° C. under nitrogen, the mixture was cooled to room temperature, shaken with aqueous sodium bicarbonate and ethyl acetate and then filtered. The organic phase was then separated and the aqueous phase was extracted twice with ethyl acetate. The combined organic phase was dried over Na2SO4, evaporated and the crude was purified on silica gel (eluant dichloromethane/methanol 97/3). 20 mg of the title compound were isolated.

Aufarbeitung

  1. temperaturethe mixture was cooled to room temperature
  2. filtrationfiltered
  3. customThe organic phase was then separated
  4. extractionthe aqueous phase was extracted twice with ethyl acetate
  5. dry with materialThe combined organic phase was dried over Na2SO4
  6. customevaporated
  7. customthe crude was purified on silica gel (eluant dichloromethane/methanol 97/3)

Quellen und Nachweise

ORD-Eintrag
ord-637d3de830b24e68ae35d15e81b4357e
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08981089B2

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