Reaktion #1283901
ord-73fd40372ad6478e9913e88106c667f5
Reaktionsgleichung
N-[1,3-dimethyl-2,4-dioxopyrimidine-6-yl]-N'-ethylethylenediamine
N-(1,3-dimethyl-2,4-dioxopyrimidine-6-yl)-N'-ethylethylenediamine
Compound 13
N-(1,3-dimethyl-2,4-dioxopyrimidine-6-yl)-N'-ethylethylenediamine
3-(3-methyl-4-oxo-4H-1-benzopyran-5-yl)oxypropyl bromide
Compound 2
3-(3-methyl-4-oxo-4H-1-benzopyran-5-yl)oxypropyl bromide
dimethyl sulfoxide
→
Edukte
N-[1,3-dimethyl-2,4-dioxopyrimidine-6-yl]-N'-ethylethylenediamine
N-(1,3-dimethyl-2,4-dioxopyrimidine-6-yl)-N'-ethylethylenediamine
Compound 13
N-(1,3-dimethyl-2,4-dioxopyrimidine-6-yl)-N'-ethylethylenediamine
3-(3-methyl-4-oxo-4H-1-benzopyran-5-yl)oxypropyl bromide
Compound 2
3-(3-methyl-4-oxo-4H-1-benzopyran-5-yl)oxypropyl bromide
dimethyl sulfoxide
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1SonstigeThe resultant reaction solution
- 2Temperaturwas cooled
- 3Filtrationthe formed white crystals were collected by filtration
- 4Waschenwashed with water
- 5Sonstigedried
Vorschrift
To 5 ml of dimethyl sulfoxide were added 0.52 g of the previously obtained N-[1,3-dimethyl-2,4-dioxopyrimidine-6-yl]-N'-ethylethylenediamine (Compound 13), 0.7 g of 3-(3-methyl-4-oxo-4H-1-benzopyran-5-yl)oxypropyl bromide (Compound 2) and 0.5 ml of triethylamine, and reaction was carried out at 100° C. for 6 hours. The resultant reaction solution was cooled, and the formed white crystals were collected by filtration, washed with water, and then dried, thereby obtaining 0.56 g of 1,3-dimethyl-6-(2-[N-ethyl-N-[3-(3-methyl-4-oxo-4H-1-benzopyran-5-yl)oxypropyl]amino]ethylamino)-2,4(1H,3H)-pyrimidinedione (the non-oxalate of Compound 14).