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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039580Generated: October 25, 2026

Triphenylphosphine → methyl (E)-3-(2-{3-[6-oxo-3-(3,4,5-trifluorophenyl)-6H-pyridazin-1-ylmethyl]phenyl}pyrimidin-5-yl)acrylate

https://huagongshe.com/reaction/2039580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactantmethyl (E)-3-[2-(3-hydroxymethylphenyl)pyrimidin-5-yl]acrylateHCID 58289762—
Reactant6-(3,4,5-trifluorophenyl)-2H-pyridazin-3-oneHCID 59406809—
SolventTetrahydrofuranHCID 8028—
Productmethyl (E)-3-(2-{3-[6-oxo-3-(3,4,5-trifluorophenyl)-6H-pyridazin-1-ylmethyl]phenyl}pyrimidin-5-yl)acrylateHCID 59484916—

Reaction Steps

47.2 90 mg (0.4 mmol) of 6-(3,4,5-trifluorophenyl)-2H-pyridazin-3-one and 111 mg (0.41 mmol) of methyl (E)-3-[2-(3-hydroxymethylphenyl)-pyrimidin-5-yl]acrylate are suspended in 3 ml of THF with 200 mg (0.6 mmol) of polymer-bound triphenylphosphine (about 3 mmol of triphenylphosphine per g), and the mixture is shaken at room temperature for 30 min. The mixture is cooled to 0° C., and 95 μl (0.6 mmol) of diethyl azodicarboxylate are added. The reaction mixture is shaken at room temperature for 24 h. The reaction mixture is purified by means of preparative HPLC; yield: 7 mg of “A283”; HPLC: Rt=3.41 min (method C);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580781B2
Source datasetuspto-grants-2013_11
ORD IDord-060fd3a423584c008ac274639ccf44e9
Source noteuspto-grants-2013_11