HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-(1-cyclopentyl-7-fluoro-1H-indazol-3-yl)phenyl phenyl hydrogen phosphate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Phosphorodichloridic acid, phenyl ester | HCID 13038 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 4-(1-cyclopentyl-7-fluoro-1H-indazol-3-yl)phenol | HCID 135524867 | — |
| Product | 4-(1-cyclopentyl-7-fluoro-1H-indazol-3-yl)phenyl phenyl hydrogen phosphate | HCID 68883427 | — |
Reaction Steps
A solution of 4-(1-cyclopentyl-7-fluoro-1H-indazol-3-yl)phenol (0.30 g, 1.0 mmol), phenyl dichlorophosphate (0.211 mL, 1.1 mmol), and lithiumhexamethyidisilazide (0.183 g, 1.1 mmol) in 10 mL of THF was stirred for 1 hour at ambient temperature. The reaction mixture was quenched with H2O and concentrated in vacuo. The residues were purified by reversed phase HPLC (Column: HS Hyperprep C18 8 u ID 22 mm; solvent gradient 40% to 100% acetonitrile (0.1% TFA) in H2O; flowrate 10 mL/min) to give 0.120 g of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241791B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-accd1b0b14634a2b9b8d7abd46b18ccb |
| Source note | uspto-grants-2007_07 |