Reaktionsgleichung
O.[NH2:2][NH2:3].Cl[C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[N:7][N:6]=1>C(O)C>[CH:11]1[CH:12]=[CH:13][C:14]2[C:9](=[CH:8][N:7]=[N:6][C:5]=2[NH:2][NH2:3])[CH:10]=1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
Again according to the disclosure in the '397 application, to a 2-L, 3-necked, round-bottomed flask fitted with a temperature probe and condenser were charged 700 mL of ethanol and 7.6 mole equivalents (630 mL) of hydrazine hydrate, and the solution was cooled to 50° C. (the '397 application discloses a temperature <10° C.). One (1) mole equivalent (280 g) of 1-chlorophthalazine (solid) was added in portions at a rate to maintain the solution temperature at <20° C. The solution was stirred and heated to 60-70° C. After one hour at that elevated temperature, the hot solution was filtered to remove any insoluble by-products (insoluble matter recovered was 12 g), and the filtrate was cooled to 0 to 5° C. A light yellow solid formed in the cold solution, which was isolated by filtration, washed with cold ethanol, and then dried to constant mass and characterized. The yield was 80% (the yield reported in the '397 application was 77-80%).
Aufarbeitung
- temperatureto maintain the solution temperature at <20° C
- temperatureheated to 60-70° C
- filtrationthe hot solution was filtered
- customto remove
- customany insoluble by-products (insoluble matter recovered was 12 g)
- temperaturethe filtrate was cooled to 0 to 5° C
- customA light yellow solid formed in the cold solution
- customwhich was isolated by filtration
- washwashed with cold ethanol
- customdried to constant mass
Quellen und Nachweise
- ORD-Eintrag
- ord-bb6d8be684774c60a3910db54716eeaf
- Quelldatensatz
- uspto-grants-2010_10
- Patentnummer
- US07807830B2
Verknüpfte Notizen
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