Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509029Generated: October 31, 2026

Cyclopentanecarboximidamide → 2-cyclopentyl-1,6,7,8-tetrahydrothiopyrano[3,2-d]pyrimidin-4-one

https://huagongshe.com/reaction/1509029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanecarboximidamideHCID 4452694—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 3-oxotetrahydrothiopyran-2-carboxylateHCID 18379299—
SolventEthanolHCID 702—
Product2-cyclopentyl-1,6,7,8-tetrahydrothiopyrano[3,2-d]pyrimidin-4-oneHCID 17851742144%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of cyclopentanecarboximidamide (3.2 g, 28.0 mmol) in ethanol (150 mL) was added methyl 3-oxotetrahydro-2H-thiopyran-2-carboxylate (4.95 g, 28.0 mmol) and sodium methoxide (1.5 g, 28.0 mmol). The mixture was stirred at 85° C. for 16 h. The ethanol was removed under vacuum and the residue was diluted with water and extracted with methylene chloride. The organic layers were dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated. The residue was diluted with hexanes and the solid was filtered to afford the title compound (2.9 g, 44%) as a white solid. MW=236.33. 1H NMR (CDCl3, 500 MHz) δ 11.41 (s, 1H), 3.13-2.99 (m, 1H), 2.99-2.94 (m, 2H), 2.81-2.70 (m, 2H), 2.21-2.14 (m, 2H), 2.14-2.04 (m, 2H), 1.92-1.79 (m, 4H), 1.73-1.64 (m, 2H); APCI MS m/z 237 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-68d64a8e58a74c3680e26ba069de36b6
Source noteuspto-grants-2015_12