HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669417Generated: October 31, 2026
Triphenylphosphine → HCID 86627897, compound
https://huagongshe.com/reaction/1669417
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 67343119 | HCID 67343119 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Product | HCID 86627897 | HCID 86627897 | — |
Reaction Steps
Methyl (7S)-14-cyclohexyl-7-hydroxy-3-(pyridin-2-ylmethoxy)-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate was dissolved in THF (60 mM) and PPh3 (1.2 eq) was added. The solution was cooled to 0° C. and treated with DIPEA (1 eq), followed by slow addition of DIAD (1.2 eq). The mixture was left stirring at this temperature for 5 min, then a solution of DPPA in THF (1.2 eq) was added dropwise. After complete addition the mixture was stirred at 0° C. for further 30 min, then stirring was continued at RT. Since no reaction was observed after 1 h more PPh3 in THF (1.2 eq), DIAD in THF (1.2 eq) and DPPA in THF (0.6 eq) were added at RT. The formation of a precipitate was observed. Stirring was continued for 1 h at RT after which time HPLC-MS indicated complete conversion. The mixture was used without further treatment in the next reaction (quant). (ES+) m/z 538 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989438B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-8f5c7751db4e40ba92fcab87b344c71f |
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| Source note | uspto-grants-2011_08 |
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