HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 66718925, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | HCID 21265914 | HCID 21265914 | — |
| Reactant | HCID 66718917 | HCID 66718917 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66718925 | HCID 66718925 | — |
Reaction Steps
To 55 mL of a tetrahydrofuran solution containing 0.39 g (2.40 mmol) of 2-(imidazo[1,2-a]pyrimidin-2-yl)ethanol obtained in Example 1-(b) were added 0.69 g (2.00 mmol) of ethyl 8-hydroxy-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-2-benzazepin-4-acetate (see WO 98/14192 A) and 0.74 g (2.80 mmol) of triphenyl-phosphine, and the mixture was stirred under ice-cooling. Then, 2.6 mL of a tetra-hydrofuran solution containing 0.53 g (2.60 mmol) of diisopropyl azodicarboxylate was added dropwise to the mixture over 3 minutes, the mixture was gradually elevated to room temperature, and stirred for 14 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377922B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-73bf32cb7b984bc3969e8e83d350b1d1 |
| Source note | uspto-grants-2013_02 |