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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422145Generated: October 31, 2026

Methyl {4,6-dichloro-2-[(4-nitrophenyl)methyl]pyrimidin-5-yl}acetate → HCID 59514483, compound

https://huagongshe.com/reaction/2422145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl {4,6-dichloro-2-[(4-nitrophenyl)methyl]pyrimidin-5-yl}acetateHCID 50878583—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59514483HCID 5951448372%

Reaction Steps

A solution of methyl[4,6-dichloro-2-(4-nitrobenzyl)pyrimidin-5-yl]acetate (2.00 g, 5.62 mmol) in anhydrous THF (50 mL) was treated with Pd/C (10% Pd, 0.200 g) and the resulting black suspension was stirred under an atmosphere of hydrogen at room temperature. After 16 hours, the reaction mixture was filtered over Celite and the residue rinsed with copious amounts of MeOH. The filtrate was concentrated in vacuo to give the crude product as a dark yellow oil which was chromatographed (silica gel, 40% EtOAc in n-hexane) to give methyl[2-(4-aminobenzyl)-4,6-dichloropyrimidin-5-yl]acetate (1.32 g, 72% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960393B2
Source datasetuspto-grants-2011_06
ORD IDord-257db6d094ff411489dd38cb3d5aa91c
Source noteuspto-grants-2011_06