Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219944Generated: November 4, 2026

2,3-Dichloropyridine → 7-(3-Chloropyridin-2-yl)-N-(4-fluorophenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-amine

https://huagongshe.com/reaction/2219944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichloropyridineHCID 16988—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59771790HCID 59771790—
Solventdioxane N,N-dimethylacetamideHCID 67000103—
Product7-(3-Chloropyridin-2-yl)-N-(4-fluorophenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-amineHCID 1200434530%

Reaction Conditions

Temperature150 °C

Reaction Steps

N-(4-Fluorophenyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-amine (0.47 g, 1.92 mmol) was dissolved in a mixture of dioxane/N,N-dimethylacetamide (4:1) (3 mL). To the mixture was added 2,3-dichloropyridine (420 mg, 2.86 mmol) and N,N-diisopropylethylamine (0.38 mL, 2.2 mmol). The mixture was heated at 150° C. in a Personal Chemistry microwave for 16 h. The solvents were removed under vacuum and the residue was dissolved in ethyl acetate and washed with sat. NaHCO3 and brine. The organic layer was dried over Na2SO4, filtered and evaporated to give a brown residue. The residue was purified by silica gel chromatography using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as an off-white powder (200 mg, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414131B2
Source datasetuspto-grants-2008_08
ORD IDord-6bfef371cb1b40bdbe5d1d240319926e
Source noteuspto-grants-2008_08