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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397175Generated: October 31, 2026

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

https://huagongshe.com/reaction/1397175

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 stifling. 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., 6 H) 8.35 (s, 1 H) 13.40 (br. s., 1 H). 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 numberUS08901147B2
Source datasetuspto-grants-2014_12
ORD IDord-6da93fec866147979c9f0d25d4c67546
Source noteuspto-grants-2014_12