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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670201Generated: October 30, 2026

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

https://huagongshe.com/reaction/1670201

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 numberUS07989477B2
Source datasetuspto-grants-2011_08
ORD IDord-76156b78f019425687d74faf0b5a72eb
Source noteuspto-grants-2011_08