HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Bromoacetyl)benzonitrile → 4-{[1-(3-Benzenesulfonyl-3-aza-bicyclo[3.1.0]hex-6-yl)-4,4-bis-(1-trityl-1H-imidazol-4-ylmethyl)-4,5-dihydro-5-oxo-1H-imidazol-2-ylsulfanyl]-acetyl}-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Bromoacetyl)benzonitrile | HCID 98654 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 3-(3-Benzenesulfonyl-3-aza-bicyclo[3.1.0]hex-6-yl)-2-thioxo-5,5-bis-(1-trityl-1H-imidazol-4-ylmethyl)-imidazolidin 4one | HCID 88218053 | — |
| Product | 4-{[1-(3-Benzenesulfonyl-3-aza-bicyclo[3.1.0]hex-6-yl)-4,4-bis-(1-trityl-1H-imidazol-4-ylmethyl)-4,5-dihydro-5-oxo-1H-imidazol-2-ylsulfanyl]-acetyl}-benzonitrile | HCID 88218079 | — |
Reaction Steps
Using the same procedure as described in Example 1C, the title compound of 53C (0.548 g, 0.558 mmol) and 4-cyanophenacyl bromide (138 mg, 0.614 mmol) in the presence of potassium bis(trimethylsilyl)-amide (129 mg, 0.614 mmol) reacted to yield the title compound of 53D, after chromatographic purification, 0.46 g (0.41 mmol, 73% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194438B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-9122f055859148baa9fe44728ab7cce2 |
| Source note | uspto-grants-2001_02 |