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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450115Generated: October 26, 2026

N-(2-Fluoro-4-iodo-phenyl)-2-pyrimidin-4-ylmethyl-malonamic acid ethyl ester → 7-(2-Fluoro-4-iodo-phenylamino)-pyrrolo[1,2-c]pyrimidine-6-carboxylic acid ethyl ester

https://huagongshe.com/reaction/450115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Fluoro-4-iodo-phenyl)-2-pyrimidin-4-ylmethyl-malonamic acid ethyl esterHCID 67234244—
ReactantHCID 178479711HCID 178479711—
SolventTolueneHCID 1140—
Product7-(2-Fluoro-4-iodo-phenylamino)-pyrrolo[1,2-c]pyrimidine-6-carboxylic acid ethyl esterHCID 6723431916.4%

Reaction Steps

To a solution of N-(2-fluoro-4-iodo-phenyl)-2-pyrimidin-4-ylmethyl-malonamic acid ethyl ester (4 g, 9.02 mmol) in toluene (120 mL) was added phosphorous (V) oxychloride (4.2 mL, 45.1 mmol). The reaction was heated at reflux for 16 hours then concentrated in vacuo. The resultant residue was dissolved in ethyl acetate (30 mL), washed with saturated aqueous sodium bicarbonate solution (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 0-40% ethyl acetate in cyclohexane) to yield a dark brown solid. The solid was triturated with ether (10 mL) to yield the title compound as a light brown solid (0.63 g, 16%). LCMS (Method B): RT=3.95 min, M+H+=426.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486963B2
Source datasetuspto-grants-2013_07
ORD IDord-e20f52c92f51455fbf65d32b2bbc7cb4
Source noteuspto-grants-2013_07