HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474212Generated: November 1, 2026
Triphenylphosphine → HCID 46836199, compound
https://huagongshe.com/reaction/474212
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | Cyclopentane-1,3-diol | HCID 100165 | — |
| Reactant | HCID 59438049 | HCID 59438049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 46836199 | HCID 46836199 | — |
Reaction Steps
100 mg (0.28 mmol) of 2-[3-(5-hydroxypyrimidin-2-yl)benzyl]-6-(1-methyl-1H-pyrazol-4-yl)-2H-pyridazin-3-one are dissolved in 6 ml of DMF, and 277 mg (0.83 mmol) of polymer-bound triphenylphosphine (3 mmol/g) and 33 mg (0.32 mmol) of 1,3-cyclopentanediol are added. The reaction mixture is shaken at room temperature for 15 min, and 196 mg (0.83 mmol) of di-tert-butyl azodicarboxylate are subsequently added. The reaction mix-ture was shaken at room temperature for 3 h, a further 277 mg (0.83 mmol) of polymer-bound triphenylphosphine (3 mmol/g) and 196 mg (0.83 mmol) of di-tert-butyl azodicarboxylate were added, and the mixture was shaken at room temperature for 18 h. The reaction mixture is filtered off through kieselguhr with suction and washed with acetonitrile. The filtrate is evaporated and purified by means of preparative HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637518B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-e9eb59344b0d42c0b317ad287184d618 |
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| Source note | uspto-grants-2014_01 |
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