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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494617Generated: October 26, 2026

HCID 178418361, compound → HCID 178471568, compound

https://huagongshe.com/reaction/1494617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178471566HCID 178471566—
CatalystPalladiumHCID 23938—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 178471568HCID 17847156823%

Reaction Steps

A solution of 84.4 mg of diethyl N-(4-[2-(2-acetamido-4-hydroxypyrido[2,3-d]pyrimidin-6-yl)prop-1-enyl]benzoyl)-L-glutamate in 30 mL of trifluoroacetic acid was hydrogenated at 55 psi of hydrogen in the presence of 0.42 g of 5% Pd/C at room temperature for 24 hours. The catalyst was removed by filtration and the filtrate was evaporated under reduced pressure. The resulting residue was taken up in chloroform and was extracted with a saturated sodium bicarbonate solution. The organic layer was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. The residue was then subjected to thin layer chromatography using a 5% methanol:chloroform mixture as the eluent. After elution of a first fraction, there was obtained 19.6 mg of the title compound, NMR (CDCl3 250 MHz), d 1.20-1.33(m, overlapping methyls, 9H), 2.45-3.36(m, 15H), 4.11(q, 2H, J=7.14 Hz), 4.23(q, 2H, J=7.10 Hz), 4.89(m, 1H), 5.44(brs, 1H), 7.24(d, 2H, J=7.54 Hz), 7.72(d, 2H, J=7.54 Hz), 9.77(brs, 1H), 11.26(brs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026851
Source datasetuspto-grants-1991_06
ORD IDord-8d00da79007f4d36aeb40cf97ec44bb8
Source noteuspto-grants-1991_06