HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-(1-Azidoethyl)-3-phenyl-1-(toluene-4-sulfonyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | 1-[3-Phenyl-1-(toluene-4-sulfonyl)-1H-indol-2-yl]ethanol | HCID 68157035 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(1-Azidoethyl)-3-phenyl-1-(toluene-4-sulfonyl)-1H-indole | HCID 86668868 | 75.2% |
Reaction Steps
A solution of DIAD (1.80 g, 8.89 mmol) in dioxane (5 mL) was added to a solution of triphenylphosphine (2.33 g, 8.89 mmol) in dioxane (20 mL) at 0° C. under a nitrogen atmosphere. After 10 min stirring, 1-[3-phenyl-1-(toluene-4-sulfonyl)-1H-indol-2-yl]ethanol (1.74 g, 4.44 mmol) in dioxane (15 mL) was added followed by diphenylphosphoryl azide (1.47 g, 5.53 mmol) in dioxane (5 mL). The reaction mixture was stirred at 20° C. for 16 h then the reaction mixture was diluted with DCM and purified by column chromatography (Si—PCC, gradient 10-100% DCM in pentane) affording the title compound as a gum (1.39 g, 75%). LCMS (Method C): RT 4.77 min [M-N3]+ 374.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-8a38f60995c7463282ff66570af9ef7a |
| Source note | uspto-grants-2014_02 |