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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984618Generated: October 26, 2026

2-Bromotoluene → 1-o-tolyl-tetrahydro-1H-pyrrolo[1,2-a]imidazole-2,5-dione

https://huagongshe.com/reaction/1984618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromotolueneHCID 7236—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantDimiracetamHCID 65955—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-o-tolyl-tetrahydro-1H-pyrrolo[1,2-a]imidazole-2,5-dioneHCID 1173636415.4%

Reaction Steps

To a solution of tetrahydro-pyrrolo[1,2-a]imidazole-2,5-dione (1.3 g, 9.28 mmol, prepared as described in J. Med. Chem. 36, 4214, 1994) in N-methylpyrrolidone (NMP, 12 cc), Cul (0.5 g, 2.62 mmol), K2CO3 (1.3 g, 9.28 mmol) and 2-bromotoluene (6 g, 35 mmol) were added under stirring. The suspension was heated in a microwave apparatus (250 Watt) for 1 h. Ethyl acetate was added to the suspension and the solid was filtered. The organic phase was washed with water and the aqueous phase was re-extracted with CH2Cl2. The organic phases were gathered and dried over Ma2SO4, filtered and concentrated to dryness. The residue was triturated with Et2O. The solid was filtered, and crystallized the first time with IPrOH and then with AcOEt to yield 0.33 g of the title compound, mp=138-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544705B2
Source datasetuspto-grants-2009_06
ORD IDord-7cc629a470e8418882b2768294ed62ac
Source noteuspto-grants-2009_06