HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60681Generated: October 25, 2026
Triphenylphosphine → HCID 117729796, compound
https://huagongshe.com/reaction/60681
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 3-Tetrahydropyranyloxy-1-propanol | HCID 10855766 | — |
| Reactant | 5-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)-2-chlorophenol | HCID 68952645 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117729796 | HCID 117729796 | 96% |
Reaction Steps
To a solution of 5-(5-amino-3-tert-butyl-pyrazol-1-yl)-2-chloro-phenol (WO2011/154734A1, which is incorporated herein by reference in it is entirety; 500 mg, 1.88 mmol), and Ph3P (986 mg, 3.76 mmol) in dry THF (10 mL) was added 3-(tetrahydro-pyran-2-yloxy)-propan-1-ol (Can. J. Chem. Vol. 73, 1195, pp 1682, which is incorporated herein by reference in it is entirety; 452 mg, 2.82 mmol). The resulting mixture was cooled to 0° C. using an ice bath and diethylazodicarboxylate (0.69 mL, 3.76 mmol) was added to the chilled mixture which was allowed to warm up to RT. The volatiles were removed under reduced pressure. The residue was purified by FCC, using 0-50% EtOAc in cyclohexane, to give the title compound (739 mg, 96%). LCMS (Method 1): Rt 3.63 min, m/z 408 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440974B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-b2337666d511490898fa66a72f17d3a1 |
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| Source note | uspto-grants-2016_09 |
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