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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631842Generated: October 27, 2026

4-Chlorophenyl isothiocyanate → N-(4-chlorophenyl)-5-fluoro-4-imino-3-methyl-2-oxo-3,4-dihydropyrimidine-1(2H)-carbothioamide

https://huagongshe.com/reaction/631842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophenyl isothiocyanateHCID 16480—
ReactantHCID 178481639HCID 178481639—
SolventDimethylformamideHCID 6228—
ProductN-(4-chlorophenyl)-5-fluoro-4-imino-3-methyl-2-oxo-3,4-dihydropyrimidine-1(2H)-carbothioamideHCID 7559336452%

Reaction Steps

1-Chloro-4-isothiocyanatobenzene (78 mg, 0.46 mmol) was added to a stirred mixture of 5-fluoro-4-imino-3-methyl-3,4-dihydropyrimidin-2(1H)-one (60 mg, 0.42 mmol) and DMF (1.0 mL) and stirred at room temperature overnight. The solvent was removed and the residue was purified on normal phase chromatography (gradient, 0 to 10% MeOH-DCM). A second purification (gradient, 2 to 6% [10% NH4OH-MeOH]-DCM) gave the title compound as a yellow gum (68 mg, 52%); 1H NMR (400 MHz, DMSO-d6) δ 11.16 (s, 1H), 10.99 (s, 1H), 7.75 (d, J=39.7 Hz, 2H), 7.48-7.15 (m, 3H), 3.22 (d, J=13.8 Hz, 3H); 13C NMR (101 MHz, DMSO-d6) 6148.96, 144.90, 138.17, 136.27, 135.90, 128.51, 124.11, 123.07, 29.88; ESIMS m/z 311 ([M−H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321734B2
Source datasetuspto-grants-2016_04
ORD IDord-15c95e963a404815a5b39870a5a30026
Source noteuspto-grants-2016_04