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HRID 522507Erstellt: 24. Oktober 2026

Caffeine → ethyl 2-((1,3,7-trimethyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-yl)methyl)acrylate

https://huagongshe.com/de/reaction/522507

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCaffeineHCID 2519—
Edukt2-(Bromomethyl)acrylic acid ethyl esterHCID 310620—
EduktLithium ChlorideHCID 433294—
EduktHCID 178418546HCID 178418546—
LösungsmittelTetrahydrofuranHCID 8028—
Produktethyl 2-((1,3,7-trimethyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-8-yl)methyl)acrylateHCID 5852653469%

Reaktionsbedingungen

Temperatur-50 °C

Reaktionsschritte

TMPZnCl.LiCl (2) (1.3 M in THF, 0.85 mL, 1.1 mmol) was added to a solution of 1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione (12) (194 mg, 1.0 mmol) in THF (2 mL) at 25° C. and the reaction mixture was then stirred at this temperature for max. 5 min. After cooling down to −50 ° C., ethyl 2-(bromomethyl)acrylate (230 mg, 1.2 mmol) and CuCN.2LiCl (1.0 M solution in THF, 5 drops) were added and the resulting mixture was allowed to warm up slowly overnight. The reaction mixture was quenched with a sat. aq. NH4Cl solution (20 mL), extracted with diethyl ether (3×50 mL) and dried over anhydrous Na2SO4. After filtration, the solvent was evaporated in vacuo. Purification by flash-chromatography (CH2Cl2/ether, 1:1) furnished compound 14b (211 mg, 69%) as a colourless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09334237B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-543c1b1ba79a4416a7ec9715cd78226f
Quellennotizuspto-grants-2016_05