HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 178499916, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Methyl 3-(4-{[(2-nitrophenyl)sulfonyl]amino}phenyl)propanoate | HCID 23157467 | — |
| Reactant | HCID 178519697 | HCID 178519697 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178499916 | HCID 178499916 | — |
Reaction Steps
To a solution of methyl 3-(4-{[(2-nitrophenyl)sulfonyl]amino}phenyl)propanoate (364 mg, 1.0 mmol), (4-{[(1E)-(4-phenyl-1,3-thiazol-2-yl)methylene]amino}phenyl)methanol (297 mg, 1.0 mmol) and triphenylphosphine (393 mg, 1.5 mmol) in tetrahydrofuran (4 mL) was added diethyl azodicarboxylate (40% toluene solution, 660 mg, 1.5 mmol) at room temperature, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was purified by silica gel column chromatography (5%-70% ethyl acetate/hexane) to give a yellow oil containing the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786165B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-095d44eed5664a7387c1f00c651ba319 |
| Source note | uspto-grants-2010_08 |