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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605Generated: October 26, 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/reaction/1605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmonium AcetateHCID 517165—
ReactantDiethyl 1-(6-chloro-1-oxoindan-2-yl)imidazole-2,4-dicarboxylateHCID 19691073—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Productethyl 7-chloro-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylateHCID 1969106761.7%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726175
Source datasetuspto-grants-1998_03
ORD IDord-e4f280544c164e7781c5e91559bf59d4
Source noteuspto-grants-1998_03