HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591964Generated: October 30, 2026
Triphenylphosphine → HCID 67139716, compound
https://huagongshe.com/reaction/1591964
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2-(4-Methoxybenzyl)-1,2,5-thiadiazolidin-3-one 1,1-dioxide | HCID 58842864 | — |
| Reactant | HCID 178418642 | HCID 178418642 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67139716 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291635B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-d92148b81b634fefb66e08fd0304b2ab |
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| Source note | uspto-grants-2007_11 |
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