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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486223Generated: October 31, 2026

Dimethylamine → pyrido[1,2-a]indol-6(7H)-one

https://huagongshe.com/reaction/486223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantFormaldehydeHCID 712—
Reactant8,9-dihydro-7-[(5-methyl-1H-imidazol-4-yl)methyl]pyrido[1,2-a]indol-6(7H)-oneHCID 10265615—
SolventAcetic AcidHCID 176—
Productpyrido[1,2-a]indol-6(7H)-oneHCID 1789325387.5%

Reaction Steps

To a mixture of aqueous 50% dimethylamine solution (0.20 ml), aqueous 35% formaldehyde solution (0.20 ml), and acetic acid (4 ml) at 15° C. was added 8,9-dihydro-7-[(5-methyl-1H-imidazol-4-yl)methyl]pyrido[1,2-a]indol-6(7H)-one (418 mg). The mixture was heated at 60°]C. for 24 hours. After evaporation of the solvent, the residue was dissolved in water, made basic with aqueous 3N sodium hydroxide solution, and extracted three times with chloroform. The chloroform layer was washed with water and brine, dried over anhydrous sodium sulfate, and evaporated in vacuo. The oil was purified by silica gel column chromatography (20% methanol-chloroform) to give 8,9-dihydro-10-[(dimethylamino)methyl]-7-(5-methyl-1H-imidazol-4-yl)methyl]pyrido[1,2-a]indol-6(7H)-one (240 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290785
Source datasetuspto-grants-1994_03
ORD IDord-a068f6fad92f43c2968b7172336dde63
Source noteuspto-grants-1994_03