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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489512Generated: October 31, 2026

Dimethylformamide → 2,3-Dihydro-3-(4-ethoxycarbonylbut-1-yl)-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole

https://huagongshe.com/reaction/1489512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2,3-Dihydro4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazoleHCID 54124030—
Reactant1-Bromo-4-ethoxy-carbonyl-butaneHCID 86751414—
Product2,3-Dihydro-3-(4-ethoxycarbonylbut-1-yl)-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazoleHCID 70338013—

Reaction Steps

0.72 g of sodium hydride are added to a suspension of 4.1 g of 2,3-dihydro-4-methyl-2-oxo-1-pyrid-3-ylmethyleneamino-1H-imidazole in 80 ml of N,N-dimethylformamide. The mixture is heated to 50°, treated with a solution of 5.22 g of 1-bromo-4-ethoxy-carbonyl-butane in 20 ml of N,N-dimethylformamide, and stirred for 30 minutes. The N,N-dimethylformamide is then removed on a rotary evaporator. The residue is treated with ethyl acetate, during which process sodium bromide precipitates. The mixture is filtered over Celite, and the filtrate is evaporated. The residue is treated with hexane, during which process crystals precipitate. The crystals are filtered off with suction and dried yielding the title compound melting at 74°-76°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679623
Source datasetuspto-grants-1997_10
ORD IDord-9f87968347104a21b315c9bcbb925c1d
Source noteuspto-grants-1997_10