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Formamidine acetate → 4(1H)-Quinazolinone

HRID 454016
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 454016
[NH2:1][C:2]1[C:7]([C:8]([O:10]CC)=O)=[CH:6][C:5](OC)=[C:4](OCC2CCN(C)CC2)[CH:3]=1.C(O)(=O)C.[CH:28](N)=[NH:29]>COCCO>[N:1]1[C:2]2[C:7](=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:8](=[O:10])[NH:29][CH:28]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 160693Formamidine acetate2×HCID 21874813Ethyl 2-amino-5-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoate

Produkt 1

HCID 1354087534(1H)-QuinazolinoneAusbeute 173,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 80192-MethoxyethanolLösungsmittel

Reaktionsbedingungen

Temperatur
115 °C

Versuchsvorschrift

A solution of ethyl 6-amino-3-methoxy-4-(1-methylpiperidin-4-ylmethoxy)benzoate (16.1 g, 50 mmol) in 2-methoxyethanol (160 ml) containing formamidine acetate (5.2 g, 50 mmol) was heated at 115° C. for 2 hours. Formamidine acetate (10.4 g, 100 mmol) was added in portions every 30 minutes during 4 hours. Heating was prolonged for 30 minutes after the last addition. After cooling, the volatiles were removed under vacuum. The solid was dissolved in ethanol (100 ml) and methylene chloride (50 ml). The precipitate was removed by filtration and the filtrate was concentrated to a final volume of 100 ml. The suspension was cooled to 5° C. and the solid was collected by filtration, washed with cold ethanol followed by ether and dried under vacuum overnight at 60° C. to give 6-methoxy-74(1-methylpiperidin-4-yl)methoxy)-3,4-dihydroquinazolin-4-one (12.7 g, 70%).

Aufarbeitung

  1. temperatureHeating
  2. additionafter the last addition
  3. temperatureAfter cooling
  4. customthe volatiles were removed under vacuum
  5. dissolutionThe solid was dissolved in ethanol (100 ml)
  6. customThe precipitate was removed by filtration
  7. concentrationthe filtrate was concentrated to a final volume of 100 ml
  8. temperatureThe suspension was cooled to 5° C.
  9. filtrationthe solid was collected by filtration
  10. washwashed with cold ethanol
  11. customdried under vacuum overnight at 60° C.

Quellen und Nachweise

ORD-Eintrag
ord-2d51471139874b3a844b51adb6d211f9
Quelldatensatz
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08492560B2

Notizen zur Reaktion

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