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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393422Generated: October 29, 2026

Methane → HCID 86753092, compound

https://huagongshe.com/reaction/2393422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHCID 18975471HCID 18975471—
SolventMethanolHCID 887—
ProductHCID 86753092HCID 86753092—

Reaction Steps

7-Chloro-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one may be prepared in the following way: 1 g of 1-[2-(6-chloro-1-oxoindanyl)]imidazole-2-carboxamide is dissolved in 50 ml of boiling methanol and, after addition of 0.1 g of decolorizing charcoal, the solution is filtered. The filter is washed with 25 ml of boiling methanol, then the filtrate and the washing are combined, 15 ml of aqueous 12N hydrochloric acid solution are added and the mixture is stored for 3 hours at 5° C. The crystals are isolated by filtration, washed twice with 20 ml in total of chilled methanol and dried under reduced pressure (1 mmHg; 0.13 kPa) at 60° C. 0.4 g of 7-chloro-5H,10H-imidazo-[1,2-a]indeno(1,2-e]pyrazin-4-one hydrochloride is thus obtained, decomposing without melting above 300° C. [NMR spectrum: (300 MHz; DMSO-d6 ; δ in ppm): 4.12 (s, 2H: --CH2 -- at 10); 7.44 (dd, J=8 and 1 Hz 1H: --H8); 7.66 (d, J=8 Hz, 1H: --H9); 7.95 and 8.25 (2 broad s, 1H each: --H of the imidazole); 8.05 (d, J=1 Hz, 1H: --H6); 12.97 (mult., 1H: --CONH--)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807859
Source datasetuspto-grants-1998_09
ORD IDord-58ac65e8e444470fbe15fd7799a5c96a
Source noteuspto-grants-1998_09