HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 45111803, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | HCID 67131070 | HCID 67131070 | — |
| Reactant | HCID 67131209 | HCID 67131209 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 45111803 | HCID 45111803 | — |
Reaction Steps
In analogy to the procedure described in example 29.2, [rac]-[2-(4-chloro-phenyl)-5,6-difluoro-2H-indazol-3-yl]-cyclohexyl-methanol (example 24.4) was reacted with 1-(4-hydroxy-phenoxy)-cyclopropanecarboxylic acid methyl ester (Hazeldine, Stuart T.; Polin, Lisa; Kushner, Juiwanna; White, Kathryn; Corbett, Thomas H.; Horwitz, Jerome P. Bioorganic & Medicinal Chemistry (2005), 13(12), 3910-3920) in the presence of tri-phenylphosphine and di-tert-butyl azodicarboxylate in THF to give the title compound as white solid. MS: m/e=567.4 [M+H4].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08008505B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-66c6896128284cbabf3737fbfde5fb7e |
| Source note | uspto-grants-2011_08 |