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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393395Generated: October 29, 2026

Ammonium Acetate → HCID 86753085, compound

https://huagongshe.com/reaction/2393395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantMethyl 3-formylbenzoateHCID 639145—
Reactant5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-oneHCID 10353549—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 86753085HCID 8675308555.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

0.5 g of 5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one and 1.47 g of 3-methoxycarbonyl-benzaldehyde are refluxed for 48 hours in the presence of 0.7 g of ammonium acetate in 30 ml of acetic anhydride. After cooling to a temperature in the region of 20° C., the precipitate formed is filtered off, washed with water and dried under reduced pressure (1 mmHg; 0.13 kPa) at 50° C. 0.53 g of 10-(3-methoxycarbonyl-benzylidene)-5H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one acetate is obtained in the form of a yellow powder, the melting point of which is greater than 260° C. (Analysis, C24H19 N3O5.0.19 H2O; % calculated C: 67.13; H: 4.46; N: 9.79; O: 18.63; % found C: 66.9; H: 4.4; N: 9.9; O: 18.6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807859
Source datasetuspto-grants-1998_09
ORD IDord-469c63ff87d74bf69ad28752e59e63ea
Source noteuspto-grants-1998_09