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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924447Generated: October 31, 2026

Diethyl P-((4-fluorophenyl)methyl)phosphonate → (E)-1-(3-tert-butyl-5-(4-fluorostyryl)-4-methoxyphenyl) dihydropyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1924447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl P-((4-fluorophenyl)methyl)phosphonateHCID 11064685—
Reactant(E)-N-(4-(3-tert-butyl-5-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-2-methoxystyryl)phenyl)methanesulfonamideHCID 25234639—
Product(E)-1-(3-tert-butyl-5-(4-fluorostyryl)-4-methoxyphenyl) dihydropyrimidine-2,4(1H,3H)-dioneHCID 25234642—

Reaction Steps

The title compound was prepared according the procedures described in Example 1, Part H and Example 1, Part I using the product obtained in Example 1, Part G (50 mg, 0.164 mmol) and diethyl 4-fluorobenzylphosphonate (40.5 mg, 0.164 mmol). The title compound was obtained as a solid (30 mg, 46%). 1H NMR (300 MHz, DMSO-d6): δ ppm 1.37 (s, 9H), 2.72 (t, J=6.6 Hz, 2H), 3.76 (s, 3H), 3.79 (t, =6.6 Hz, 2H), 7.21 (m, 4H), 7.30 (d, J=16.3 Hz, 1H), 7.53 (d, J=2.6 Hz, 1H), 7.73 (m, 2H), 10.35 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178548B2
Source datasetuspto-grants-2012_05
ORD IDord-f77eda5c3a574db889d96bd580630995
Source noteuspto-grants-2012_05