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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668835Generated: October 31, 2026

Diisopropylethylamine → benzyl-(2-chloro-6,7-dihydro-5H-cyclopentapyrimidin-4-yl)-ethyl-amine

https://huagongshe.com/reaction/1668835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantN-EthylbenzylamineHCID 84352—
Reactant2,4-dichloro-5H,6H,7H-cyclopenta(d)pyrimidineHCID 231331—
SolventEthanolHCID 702—
Productbenzyl-(2-chloro-6,7-dihydro-5H-cyclopentapyrimidin-4-yl)-ethyl-amineHCID 5936293399.3%

Reaction Conditions

Temperature27.5 °C

Reaction Steps

A mixture of 2,4-dichloro-6,7-dihydro-5H-cyclopentapyrimidine (0.4 g, 2.1 mmol), N-benzyl-ethylamine (0.35 mL, 2.3 mmol) and diisopropylethylamine (0.4 mL, 2.1 mmol) in anhydrous ethanol (5 mL) was heated at a temperature in the range of 20° C. to 90° C. for 18 hours. After cooling to about 20 to 35° C., the reaction mixture was concentrated under reduced pressure. The crude residue was diluted with ethyl acetate, washed with water, brine, dried over sodium sulfate, filtered and concentrated under reduced pressure to afford a light pink liquid (0.60 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989463B2
Source datasetuspto-grants-2011_08
ORD IDord-8e00028cc6cc4a17b9db62d21a41660a
Source noteuspto-grants-2011_08