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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774433Generated: October 25, 2026

Ethyl 2-(benzyloxy)-3-oxopropanoate → HCID 178517543, compound

https://huagongshe.com/reaction/1774433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(benzyloxy)-3-oxopropanoateHCID 19903223—
Reactant2-Chloropyridine-4-carboximidamideHCID 50988635—
SolventEthanolHCID 702—
ProductHCID 178517543HCID 17851754366%

Reaction Steps

A mixture of crude ethyl 2-(benzyloxy)-3-oxopropanoate (all from previous step), 2-chloropyridine-4-carboximidamide (9.57 g, 50 mmol) and 100 mL of anhydrous ethanol was refluxed for 4 h under nitrogen. The mixture was then cooled and the volatile solvents were removed by rotary-evaporator. The residue was re-dissolved in water and filtered. The filtrate was acidified by HCl (4N aq) in an ice bath and the white precipitate was filtered, washed with water, and dried to give 5-(benzyloxy)-2-(2-chloropyridin-4-yl)pyrimidin-4-ol (10.4 g, 66%). 1H NMR δ (400 MHz, d6-DMSO): 13.12 (s, 1H), 8.58 (d, J=5.2 Hz, 1H), 8.12 (s, 1H), 8.04 (d, J=5.2 Hz, 1H), 7.94 (s, 1H), 7.51-7.34 (m, 5H), 5.20 (s, 2H); MS (ESI) m/z (M++H)+ 314.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260413B2
Source datasetuspto-grants-2016_02
ORD IDord-c8e27d6be1ba40568755340dbf21efba
Source noteuspto-grants-2016_02