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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161655Generated: October 30, 2026

Cycloheptylamine → 6-chloro-N2-(3-chloro-4-methoxy-phenyl)-N4-cycloheptyl-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/1161655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCycloheptylamineHCID 2899—
ReactantTriethylamineHCID 8471—
Reactant(3-Chloro-4-methoxy-phenyl)-(4,6-dichloro-pyrimidin-2-yl)-amineHCID 58626087—
Solvent1-ButanolHCID 263—
Product6-chloro-N2-(3-chloro-4-methoxy-phenyl)-N4-cycloheptyl-pyrimidine-2,4-diamineHCID 5862607660%

Reaction Steps

To a solution of compound (3-chloro-4-methoxy-phenyl)-(4,6-dichloro-pyrimidin-2-yl)-amine (0.08 g, 0.26 mmol) in butanol (3 mL) was added to cycloheptylamine (0.03 g, 0.26 mmol) at 25° C. with stirring. To this was added triethylamine (0.14 mL, 1.04 mmol), and the mixture was stirred for 30 minutes at 25° C. and then heated and refluxed for 12 hours under nitrogen atmosphere. The mixture was concentrated under vacuum, diluted with cold water, and extracted with ethyl acetate. The organic layers were collected, combined, washed with brine, dried over anhydrous sodium sulphate, and concentrated under vacuum to give the desired compound. Yield: 60%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820654B2
Source datasetuspto-grants-2010_10
ORD IDord-6e5260e4ff7e44e7abdb032391bb80f7
Source noteuspto-grants-2010_10