Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 9855722 | HCID 9855722 | — |
| Reactant | 2-Hydroxymethyl-5-phenyl-benzofuran | HCID 11379094 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 131724969 | HCID 131724969 | — |
Reaction Steps
To a solution of 4-amino-biphenyl-3-carbonitrile (1.2 g, 6.33 mmol) and pyridine (2 mL, 25.3 mmol) was added 20% phosgene in toluene (5.7 mL(10.8 mmol) and the mixture was heated to 90° C. for 2 hrs. The mixture was filtered and the filtrate was concentrated to dryness. The crude material was dissolved in THF, and (5-phenyl-benzofuran-2-yl)-methanol (0.52 g, 2.3 mmol) and triethylamine (0.70 g, 6.9 mmol) were added. The mixture was heated at 50° C. for 15 h. The solvent was evaporated to dryness. Purification by chromatography gave 0.78 g of 3-cyano-biphenyl-4-yl)-carbamic acid-5-phenyl-benzofuran-2-yl-methyl ester as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06903086B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-666cc9a4d0854affa00fa834defaaf51 |
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| Source note | uspto-grants-2005_06 |
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