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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450114Generated: November 1, 2026

Potassium Hydroxide → N-(2-Fluoro-4-iodo-phenyl)-2-pyrimidin-4-ylmethyl-malonamic acid ethyl ester

https://huagongshe.com/reaction/450114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-(Chloromethyl)pyrimidineHCID 13123553—
ReactantN-(2-Fluoro-4-iodo-phenyl)-malonamic acid ethyl esterHCID 67234460—
ProductN-(2-Fluoro-4-iodo-phenyl)-2-pyrimidin-4-ylmethyl-malonamic acid ethyl esterHCID 6723424440%

Reaction Steps

N-(2-Fluoro-4-iodo-phenyl)-malonamic acid ethyl ester (20.5 g, 58.4 mmol), 4-chloromethyl-pyrimidine (5.0 g, 38.9 mmol) and potassium hydroxide (3.28 g, 58.4 mmol) were dissolved in IMS (200 mL). The reaction mixture was stirred at room temperature for 16 hours then concentrated in vacuo. The resultant residue was dissolved in ethyl acetate (30 mL), washed with water (20 mL) and the aqueous fraction extracted twice with ethyl acetate (2×10 mL). The combined organic fractions were washed with brine, dried (MgSO4) and concentrated in vacuo. The resultant residue was subjected to flash chromatography (SiO2, gradient 10-40% ethyl acetate in cyclohexane) to yield the title compound as an off-white solid (6.9 g, 39%). LCMS (Method B): RT=3.29 min, M+H+=444.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486963B2
Source datasetuspto-grants-2013_07
ORD IDord-c7e31450bb88434181654ae2ffe64e7d
Source noteuspto-grants-2013_07