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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636815Generated: October 30, 2026

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

https://huagongshe.com/reaction/636815

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromoacetyl)benzonitrileHCID 98654—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant3-(3-Benzenesulfonyl-3-aza-bicyclo[3.1.0]hex-6-yl)-2-thioxo-5,5-bis-(1-trityl-1H-imidazol-4-ylmethyl)-imidazolidin 4oneHCID 88218053—
Product4-{[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}-benzonitrileHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194438B1
Source datasetuspto-grants-2001_02
ORD IDord-9122f055859148baa9fe44728ab7cce2
Source noteuspto-grants-2001_02