4-Aminobenzonitrile → 7-Acetoxy-4-(4-cyanoanilino)-6,7-dihydro-5H-cyclopenta[d]pyrimidine

HRID 579747Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 579747
[C:1]([O:4][CH:5]1[C:9]2[N:10]=[CH:11][N:12]=[C:13](Cl)[C:8]=2[CH2:7][CH2:6]1)(=[O:3])[CH3:2].[NH2:15][C:16]1[CH:23]=[CH:22][C:19]([C:20]#[N:21])=[CH:18][CH:17]=1>C(O)C>[C:1]([O:4][CH:5]1[C:9]2[N:10]=[CH:11][N:12]=[C:13]([NH:15][C:16]3[CH:23]=[CH:22][C:19]([C:20]#[N:21])=[CH:18][CH:17]=3)[C:8]=2[CH2:7][CH2:6]1)(=[O:3])[CH3:2]

Komponenten

4

Edukt 2

HCID 133964-AminobenzonitrileHCID 199689354-chloro-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-yl acetate

Produkt 1

HCID 139132267-Acetoxy-4-(4-cyanoanilino)-6,7-dihydro-5H-cyclopenta[d]pyrimidineAusbeute 55,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

39.3 g of 7-acetoxy-4-chloro-6,7-dihydro-5H-cyclopenta[d]pyrimidine [prepared as described in step (b) above] and 24 g of p-aminobenzonitrile were dissolved in 180 ml of ethanol, and the solution was heated under reflux for 1.5 hours. At the end of this time, the solvent was evaporated off under reduced pressure, and the resulting residue was washed with a 1:1 by volume mixture of ethanol and toluene, to give 30 g of the title compound as pale grayish crystals, melting at 215°-217° C.

Aufarbeitung

  1. temperaturethe solution was heated
  2. temperatureunder reflux for 1.5 hours
  3. customAt the end of this time, the solvent was evaporated off under reduced pressure
  4. washthe resulting residue was washed with a 1:1 by volume mixture of ethanol and toluene

Quellen und Nachweise

ORD-Eintrag
ord-064491002d1040118ff9c94364c8cb47
Quelldatensatz
uspto-grants-1988_06
Patentnummer
US04749704

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