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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373948Generated: October 31, 2026

Diglyme → 6-(2-Fluoro-4-nitrophenoxy)-N-(4-methoxybenzyl)pyrimidin-4-amine

https://huagongshe.com/reaction/2373948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiglymeHCID 8150—
Reactant2-Fluoro-4-nitrophenolHCID 9825—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloro-N-(4-methoxybenzyl)pyrimidin-4-amineHCID 22309497—
SolventEthyl AcetateHCID 8857—
Product6-(2-Fluoro-4-nitrophenoxy)-N-(4-methoxybenzyl)pyrimidin-4-amineHCID 5930160576%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of N-(4-methoxybenzyl)-6-chloropyrimidin-4-amine (2.3 g, 9.2 mmol), 2-fluoro-4-nitrophenol (1.45 g, 9.2 mmol), DIPEA (15 mL), and 2-methoxyethyl ether (75 mL) was heated at 160° C. in a sealed pressure bottle for 50 h. The mixture was cooled, poured onto crushed ice (200 g), treated with EtOAc (200 mL). After vigorously stirring for 10 min, the insoluble material was filtered off. The EtOAc phase was washed with saturated aq. Na2CO3 solution (100 mL), brine (3×100 mL), dried (MgSO4) and concentrated in vacuo. The gummy solid obtained was triturated with isopropyl ether to give the title compound (1.75 g, 76%) as a brown solid. 1H NMR (DMSO-d6) δ 8.32 (dd, 1H, J=10.2, 2.0 Hz), 8.15 (d, 2H, J=9.2 Hz), 8.05 (br s, 1H), 7.61 (dd, 1H, J=8.4, 8.4 Hz), 7.26 (d, 2H, J=8.5 Hz), 6.91 (d, 2H, J=8.5 Hz), 6.14 (br s, 1H), 4.48 (br s, 2H), 3.74 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459562B2
Source datasetuspto-grants-2008_12
ORD IDord-8516f2e036864fd0b615a42833b6c8f5
Source noteuspto-grants-2008_12