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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19630Generated: October 26, 2026

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

https://huagongshe.com/reaction/19630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichloropyridineHCID 16988—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(6-(Trifluoromethyl)pyridin-3-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amineHCID 59346451—
Solventdioxane N,N-dimethylacetamideHCID 67000103—
Product6-(3-Chloropyridin-2-yl)-N-(6-(trifluoromethyl)pyridin-3-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amineHCID 5934654128%

Reaction Conditions

Temperature150 °C

Reaction Steps

N-(6-(Trifluoromethyl)pyridin-3-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine (130 mg, 0.44 mmol) was dissolved in a mixture of dioxane/N,N-dimethylacetamide (4:1) (2 mL). To the mixture was added 2,3-dichloropyridine (98 mg, 0.66 mmol) and N,N-diisopropylethylamine (0.11 mL, 0.66 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 using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as an off-white powder (50 mg, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745451B2
Source datasetuspto-grants-2010_06
ORD IDord-61a00e1c7bf64add85edd2fb46139082
Source noteuspto-grants-2010_06