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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359772Generated: October 31, 2026

Hydrochloric Acid → 5-acetyl-2-(methylthio)pyrimidin-4(3H)-one

https://huagongshe.com/reaction/2359772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant5-Acetyl-2-sulfanylidene-2,3-dihydropyrimidin-4(1H)-oneHCID 12755561—
Product5-acetyl-2-(methylthio)pyrimidin-4(3H)-oneHCID 5669898369.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

5-Acetyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one (Ryan Scientific) (2.3 g, 13.51 mmol) was dissolved in NaOH (20.27 mL, 20.27 mmol), then MeI (0.894 mL, 14.30 mmol) was added to the reaction mixture while stirring. The reaction mixture was heated at 40° C. for 1.5 hours. Additional MeI (0.894 mL, 14.30 mmol) was added and the reaction was allowed to stir at rt for 18 hours. The reaction mixture was cooled with an ice-water bath, acidified to pH 6 with concentrated HCl solution, then the resulting precipitate was filtered to obtain 1.72 g of the desired product (69% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 2.49 (br. s., 6H) 8.35 (s, 1H) 13.40 (br. s., 1H). MS (ES+): m/z=185.1 (100) [MH+]. HPLC: tR=1.0 minute over 3 minutes. Purity: >90% [HPLC (LC/MS) at 220 nm].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685993B2
Source datasetuspto-grants-2014_04
ORD IDord-9d96ea510c4a47a7b6f7643f25ca6763
Source noteuspto-grants-2014_04