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HRID 3661Erstellt: 23. Oktober 2026

4-Methylmorpholine → HCID 178418271, Verbindung

https://huagongshe.com/de/reaction/3661

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktIsobutyl chloroformateHCID 62365—
Edukt1,3-Diallyl-5,6-diaminouracilHCID 13525062—
Edukttrans-2-Phenyl-cyclopentanecarboxylic acidHCID 22884010—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttrans-2-Phenyl-cyclopentanecarboxylic acidHCID 22884010—
ProduktHCID 178418271HCID 17841827187,8%

Reaktionsschritte

Dissolve trans-2-phenyl-cyclopentanecarboxylic acid (1.0 g, 5.3 mmol), prepared according to F. G. Bordwell and J. Almy, J. Org. Chem., 38, 571 (1973), in tetrahydrofuran (20 ml) and add N-methylmorpholine (0.58 ml, 5.3 mmol). Cool the reaction to -20° C. and add isobutyl chloroformate (0.69 ml, 5.3 mmol). Stir the reaction for 30 minutes, add 1,3-diallyl-5,6-diaminouracil (1.2 g, 5.3 mmol, in 4 ml dimethylformamide) and stir at -20° C. for 3 hours. Warm to room temperature and dilute the reaction with diethyl ether (400 ml). Separate the layers and rinse the organic layer with saturated sodium bicarbonate (2×200 ml), 50% aqueous sodium chloride (2×300 ml), dry over anhydrous magnesium sulfate, filter and concentrate under vacuum. Purify the residue by radial chromatography (2% to 5% methanol/chloroform, 2 mm plate) to provide trans-2-phenyl-cyclo-pentanecarboxylic acid (3,5-diallyl-2-amino-4,6-dioxo-cyclohex-1-enylamide (0.51 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05734052
Quelldatensatzuspto-grants-1998_03
ORD IDord-ee021fa8c0fc47e48b1fbf4ceb821807
Quellennotizuspto-grants-1998_03