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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591964Generated: October 30, 2026

Triphenylphosphine → HCID 67139716, compound

https://huagongshe.com/reaction/1591964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant2-(4-Methoxybenzyl)-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 58842864—
ReactantHCID 178418642HCID 178418642—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67139716HCID 67139716—

Reaction Steps

The title B compound, 2-(4-methoxybenzyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (128 mg, 0.5 mmol), 4-hydroxypyridine (109 mg, 1 mmol) and triphenylphosphine (262 mg, 1 mmol) are put into a small reaction vessel under argon and dissolved in 10 mL of THF. This solution is stirred in an ice/water bath and diethyl azodicarboxylate (174 mg, 1 mmol) diluted with an equal volume of THF is added dropwise to the stirred cold solution. The reaction is allowed to stir 16 h while the ice bath slowly warms to RT. The solvent is evaporated on the rotary evaporator, then the residue is taken up in a minimal amount of CH2Cl2 and chromatographed on a 10 g RediSep silica gel column, using a gradient from 1 to 5% EtOAc in CH2Cl2 over 15 to 20 min to afford 2-(4-methoxybenzyl)-1,1-dioxo-5-pyridin-4-ylmethyl-1,2,5-thiadiazolidin-3-one: [M+1]+=348.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291635B2
Source datasetuspto-grants-2007_11
ORD IDord-d92148b81b634fefb66e08fd0304b2ab
Source noteuspto-grants-2007_11