Cyclopropylamine → HCID 178471863, Verbindung

HRID 1090388Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1090388
[C:1]([NH:4][CH:5]1[CH2:9][CH2:8][CH:7]([C:10]2[C:15]([F:16])=[CH:14][C:13]([C:17](=[O:28])[C:18](=[CH:24]OCC)[C:19]([O:21][CH2:22][CH3:23])=[O:20])=[C:12]([F:29])[CH:11]=2)[CH2:6]1)(=[O:3])[CH3:2].[CH:30]1([NH2:33])[CH2:32][CH2:31]1>C(O)C>[C:1]([NH:4][CH:5]1[CH2:9][CH2:8][CH:7]([C:10]2[C:15]([F:16])=[CH:14][C:13]([C:17](=[O:28])[C:18](=[CH:24][NH:33][CH:30]3[CH2:32][CH2:31]3)[C:19]([O:21][CH2:22][CH3:23])=[O:20])=[C:12]([F:29])[CH:11]=2)[CH2:6]1)(=[O:3])[CH3:2]

Komponenten

4

Edukt 2

HCID 69828CyclopropylamineHCID 86743970HCID 86743970, Verbindung

Produkt 1

HCID 178471863HCID 178471863, VerbindungAusbeute 76,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A solution of 20.5 g (50 mmol) of 4-[3-(acetylamino)cyclopentyl]-α-(ethoxymethylene)-2,5-difluoro-β-oxobenzenepropanoic acid, ethyl ester, in 100 ml of absolute ethanol was cooled to 10° and 3.4 g (60 mmole) of cyclopropylamine was added dropwise maintaining the temperature below 15° with an ice bath. After the addition was complete, the reaction was stirred at 5°-10° for 1.5 hours and then at room temperature for 1 hour. The resulting suspension was chilled to 5° and the solid removed by filtration and washed with ethanol and then hexane. The combined filtrate and washings were evaporated in vacuo and the residue was recrystallized from pentane to give 16.1 g of the title compound.

Aufarbeitung

  1. temperaturemaintaining the temperature below 15° with an ice bath
  2. additionAfter the addition
  3. waitat room temperature for 1 hour
  4. temperatureThe resulting suspension was chilled to 5°
  5. customthe solid removed by filtration
  6. washwashed with ethanol
  7. customThe combined filtrate and washings were evaporated in vacuo
  8. customthe residue was recrystallized from pentane

Quellen und Nachweise

ORD-Eintrag
ord-966585e67adf4a178b47782fa2e32141
Quelldatensatz
uspto-grants-1992_01
Patentnummer
US05081254

Notizen zur Reaktion

Wird geladen…