HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366800Generated: November 1, 2026
Triphenylphosphine → HCID 59743158, compound
https://huagongshe.com/reaction/1366800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 59743156 | HCID 59743156 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59743158 | HCID 59743158 | 88% |
Reaction Steps
To a solution of 2.55 g (9.7 mmol) triphenylphosphine in 250 ml THF is added at a temperature of 0° C. 2.25 g (9.7 mmol) diterbutylazodicarboxylate in 25 ml THF. The solution is stirred for 1 hour at a temperature of 0° C. Then 0.35 ml (4.85 mmol) thioacetic acid is added and a white suspension is formed immediately. After that, a solution of 2.5 g (4.85 mmol) 2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid [4-chloro-2-(2-hydroxy-propylcarbamoyl)-6-methyl-phenyl]-amide in 30 ml THF is slowly added at a temperature of 0° C. The solution is stirred for 1 hour at a temperature of 0° C., and then 15 hours at 25° C., and then evaporated. The residue is submitted to flash-chromatography (ethyl acetate 1, hexane 2) to give 2.45 g (88%) white crystals (m.p. 137-139° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893092B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-824116a346f049c6862836e3fa0e2444 |
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| Source note | uspto-grants-2011_02 |
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