HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dichlorophenol → 1-[(2S,3R)-2-benzyloxy-5-(3,4-dichlorophenoxy)-3-pentyl]imidazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dichlorophenol | HCID 7258 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 1-[(2S,3R)-2-benzyloxy-5-hydroxy-3-pentyl]imidazole-4-carboxamide | HCID 69527311 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[(2S,3R)-2-benzyloxy-5-(3,4-dichlorophenoxy)-3-pentyl]imidazole-4-carboxamide | HCID 10160936 | 102% |
Reaction Steps
To a stirred mixture of 3,4-dichlorophenol (129 mg, 0.791 mmol), 1-[(2S,3R)-2-benzyloxy-5-hydroxy-3-pentyl]imidazole-4-carboxamide (80 mg, 0.264 mmol), and triphenylphosphine (90 mg, 0.343 mmol) in tetrahydrofuran (5 ml) was added dropwise diethyl azodicarboxylate (59.7 mg, 0.343 mmol) at ice-bath temperature. After the mixture was stirred for 2 h at room temperature, the solvent was removed in vacuo. The residue was purified by silica gel (10 g) chromatography eluting with chloroform/methanol (100:1 to 30:1) to give a mixture (120.6 mg, 102%) of 1-[(2S,3R)-2-benzyloxy-5-(3,4-dichlorophenoxy)-3-pentyl]imidazole-4-carboxamide (3) and by-products. This material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07064144B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-dc2d7060331c4b4caa6ef2be32a7f126 |
| Source note | uspto-grants-2006_06 |