Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | diazenedicarboxylic acid bis(N,N-piperidide) | HCID 5702657 | — |
| Reactant | HCID 69216007 | HCID 69216007 | — |
| Reactant | HCID 178519806 | HCID 178519806 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86605845 | HCID 86605845 | 58% |
Reaction Steps
To a mixture of methyl 4-{4-[(4-hydroxymethyl-2-methoxyphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}benzoate (0.77 g), 3-hydroxy-1-phenyl-1H-pyrazole-4-carbaldehyde (0.41 g), tributylphosphine (0.61 g) and tetrahydrofuran (100 mL) was added 1,1-(azodicarbonyl)dipiperidine (0.76 g) at room temperature, and the mixture was stirred for 15 hrs. The precipitated crystals were removed by filtration and the filtrate was concentrated. The residue was subjected to silica gel column chromatography to give methyl 4-{4-[(4-{[(4-formyl-1-phenyl-1H-pyrazol-3-yl)oxy]methyl}-2-methoxyphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}benzoate as colorless crystals (0.64 g, yield 58%) from a fraction eluted with ethyl acetate-hexane (2:1, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 190-191° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07368578B2 |
|---|
| Source dataset | uspto-grants-2008_05 |
|---|
| ORD ID | ord-a21f981d92ca40a58e128b5ba593449f |
|---|
| Source note | uspto-grants-2008_05 |
|---|