HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N'-[[2'-[(t-butylamino)sulfonyl]-1,1'-biphenyl-4-yl]methyl]-N'-heptyl-N-(2,4,6-trifluorophenyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2,4,6-Trifluorobenzoic acid | HCID 520373 | — |
| Reactant | N-[[2'-[(t-butylamino)sulfonyl]-1,1'-biphenyl-4-yl]methyl]-N-heptylamine | HCID 68851407 | — |
| Product | N'-[[2'-[(t-butylamino)sulfonyl]-1,1'-biphenyl-4-yl]methyl]-N'-heptyl-N-(2,4,6-trifluorophenyl)urea | HCID 68851965 | 81% |
Reaction Steps
Using 2,4,6-trifluorobenzoic acid (0.27 g), diphenylphosphoryl azide (0.44 g), triethylamine (0.17 g) and N-[[2′-[(t-butylamino)sulfonyl]-1,1′-biphenyl-4-yl]methyl]-N-heptylamine (0.43 g), N′-[[2′-[(t-butylamino)sulfonyl]-1,1′-biphenyl-4-yl]methyl]-N′-heptyl-N-(2,4,6-trifluorophenyl)urea was afforded as colorless crystals (0.49 g) by a similar procedure as in Example 4. Yield: 81%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531576B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-93713c4e2de840a385d60127aa87377e |
| Source note | uspto-grants-2009_05 |