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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726908Generated: November 1, 2026

HCID 57565029, compound → HCID 57565063, compound

https://huagongshe.com/reaction/1726908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57565029HCID 57565029—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 57565063HCID 57565063100.2%

Reaction Steps

A solution of ethyl 6-(benzyloxy)-1-(2-hydroxyethyl)-5-oxo-1,2,3,5-tetrahydroimidazo[1,2-a]pyrimidine-7-carboxylate (1.40 g, 3.89 mmol) in a mixture of ethyl acetate (300 ml) and ethanol (75 ml) at 25° C. was hydrogenated over 10% palladium on activated carbon (200 mg) and under one atmosphere of hydrogen for four hours to give 1.05 g (100% yield) of the title compound as light yellow needles; mp 155-156° C. (ethyl acetate). 1HNMR 400 MHz (CDCl3) δ (ppm): 1.44 (3H, t, J=7.1 Hz, CH3), 3.46 (2H, m, CH2), 3.75 (2H, t, J=8.3 Hz, CH2), 3.92 (2H, m, CH2), 4.20 (2H, t, J=8.3 Hz, CH2), 4.43 (2H, q, J=7.1 Hz, OCH2), 10.20 (1H, s, OH). Anal. Calcd for C11H15N3O5: C, 49.06; H, 5.61; N, 15.60. Found: C, 49.09, H, 5.73; N, 15.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494984B2
Source datasetuspto-grants-2009_02
ORD IDord-289f46c03f6143c09dbf19ad1ced0e3e
Source noteuspto-grants-2009_02