HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607417Generated: October 30, 2026
P,P-Diphenylphosphinic azide → HCID 178445900, compound
https://huagongshe.com/reaction/1607417
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (+/-)-2-(1-Naphthylmethyl)-5-phenyl-4-pentenoic acid | HCID 53925726 | — |
| Reactant | HCID 178445905 | HCID 178445905 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178445900 | HCID 178445900 | — |
Reaction Steps
To a solution of 190 mg of (±)-2-(1-naphthylmethyl)-5-phenyl-4-pentenoic acid and 400 mg of bis(P-toluenesulfonic acid) salt of L-histidyl-L-leucinal semicarbazone in 7 ml of N,N-dimethylformamide were successively added 0.16 ml of diphenylphosphoryl azide and 0.28 ml of triethylamine under ice-cooling, and the mixture was stirred overnight. To the reaction mixture was added a 5% aqueous sodium bicarbonate solution, and the mixture was extracted withh ethyl acetate and washed with water. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography (eluent: chloroform/methanol=15/1 by volume) to obtain 151 mg of N-[(±)-2-(1-naphthylmethyl)-5-phenyl-4-pentenoyl]-L-histidyl-L-leucinal semicarbazone as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04863904 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-c7a7a68bbcd7411991d531ef0d1bc376 |
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| Source note | uspto-grants-1989_09 |
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