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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508928Generated: October 30, 2026

Cyclopentanecarboximidamide → 2-cyclopentyl-6-ethylpyrimidin-4(3H)-one

https://huagongshe.com/reaction/1508928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanecarboximidamideHCID 4452694—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
Product2-cyclopentyl-6-ethylpyrimidin-4(3H)-oneHCID 136085107122.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

A solution of cyclopentanecarboximidamide (8.5 g, 75.8 mmol) in ethanol (150 mL) was treated with ethyl propionaylacetate (13.7 g, 94.7 mmol), followed by the addition of sodium methoxide (4.9 g, 90.9 mmol). The mixture was then heated to 85° C. overnight. After this time, the mixture was cooled and concentrated to a volume of approximately 50 mL. Then, 2M HCl in EtOH (68 mL) was added slowly. The resulting precipitate was filtered, washed with water and ether, and the residue was dried on a high vacuum overnight to afford the title compound (8.9 g, crude) as a pink solid. MW=192.26. 1H NMR (DMSO-d6, 500 MHz) δ 12.00 (s, 1H), 6.14 (s, 1H), 3.01 (quin, J=8.0 Hz, 1H), 2.55 (q, J=7.5 Hz, 2H), 2.13-2.01 (m, 2H), 1.94-1.77 (m, 4H), 1.74-1.63 (m, 2H), 1.22 (t, J=7.5 Hz, 3H); APCI MS m/z 193 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-2c6b09dd64c44289b2bfea8336472c71
Source noteuspto-grants-2015_12