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HRID 1605Erstellt: 23. Oktober 2026

Acetic Acid → ethyl 7-chloro-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate

https://huagongshe.com/de/reaction/1605

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktAmmonium AcetateHCID 517165—
EduktDiethyl 1-(6-chloro-1-oxoindan-2-yl)imidazole-2,4-dicarboxylateHCID 19691073—
LösungsmittelAcetoneHCID 180—
LösungsmittelMethanolHCID 887—
LösungsmittelAcetonitrileHCID 6342—
Produktethyl 7-chloro-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylateHCID 1969106761,7%

Reaktionsschritte

The procedure is as in Example 1 but starting from 5 g of diethyl 1-(6-chloro-1-oxoindan-2-yl)imidazole-2,4-dicarboxylate, 118 g of ammonium acetate and 190 ml of acetic acid. After washing the precipitate with water and then with methyl ethyl ketone, the solid obtained is first of all ground in acetonitrile and then in methanol and finally in acetone to obtain 2.7 g of ethyl 7-chloro-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate in the form of a brown solid melting above 260° C. (analysis % calculated C: 58.28, H: 3.67, Cl: 10.75, N: 12.74; % found C: 58.6, H: 3.4, Cl: 10.4, N: 13.1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726175
Quelldatensatzuspto-grants-1998_03
ORD IDord-e4f280544c164e7781c5e91559bf59d4
Quellennotizuspto-grants-1998_03