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HRID 15112Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/15112

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromotolueneHCID 7236—
EduktEthyl AcetateHCID 8857—
EduktPotassium CarbonateHCID 11430—
EduktDimiracetamHCID 65955—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt1-o-tolyl-tetrahydro-1H-pyrrolo[1,2-a]imidazole-2,5-dioneHCID 1173636415,4%

Reaktionsschritte

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), CuI (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 Na2SO4, 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732473B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-a5af9ae55cd3492eb5a25286165b4309
Quellennotizuspto-grants-2010_06