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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481451Generated: October 25, 2026

Dimethylformamide → 5-phenylvalerylamino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one

https://huagongshe.com/reaction/481451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDichloromethaneHCID 6344—
ReactantBenzenepentanoic acidHCID 16757—
ReactantThionyl ChlorideHCID 24386—
Reactant8-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-oneHCID 18975394—
Product5-phenylvalerylamino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-oneHCID 86752968—

Reaction Steps

The preparation is carried out as in Example 12, from 5 g of 5-phenylvaleric acid, 2.5 ml of thionyl chloride, 60 ml of dichloromethane, 1 g of 8-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one and 75 ml of dimethylformamide. After refluxing for 7 hours, the insoluble material is filtered and recrystallized from dimethylformamide. After filtration, washing with water and drying under reduced pressure (1 mm Hg, 0.13 kPa) at 80° C., there is obtained 0.58 g of 8-(5-phenylvalerylamino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one in the form of a yellow solid which decomposes at 170° C. (Analysis C24H22N4O2.0.41DMF, % calculated C: 72.34, H: 5.56, N: 14.06, % found C: 72.0, H: 5.6, N: 13.8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789406
Source datasetuspto-grants-1998_08
ORD IDord-3d88c839167a4ddaaf5796f47fd5cd1a
Source noteuspto-grants-1998_08