HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804665Generated: October 31, 2026
HCID 178435595, compound → HCID 178452388, compound
https://huagongshe.com/reaction/1804665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178435595 | HCID 178435595 | — |
| Reactant | HCID 178525131 | HCID 178525131 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178419050 | HCID 178419050 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178452388 | HCID 178452388 | 7,893.4% |
Reaction Steps
To a stirring solution of (S)-2-(5-ethynyl-1H-benzoimidazol-2-yl)-piperazine-1,4-dicarboxylic acid 1-benzyl ester 4-tert-butyl ester (77 mg, 0.16 mmol), (S)-2-(5-iodo-1H-benzoimidazol-2-yl)-piperidine-1-carboxylic acid benzyl ester (70 mg, 0.15 mmol), CuI (3 mg, 0.015 mmol) and bis(triphenylphosphine)palladium (II) dichloride (10.6 mg, 0.015 mmol) in DMF (2 mL) is added TEA (0.1 mL, 0.76 mmol). The reaction mixture is stirred at room temperature for 2 hours, diluted with EtOAc and water. The mixture is filtered to remove insoluble material and the layers of the filtrate are separated. The organic layer is dried over sodium sulfate and concentrated in vacuum to dryness. The residue is purified by flash column chromatography on silica gel (MeOH/DCM 0% to 20%) and repurified by reverse phase HPLC using a gradient of CH3CN/water to give the title compound (9.4 g, 7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08354419B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-c6591f90975e48ccbaef32550e95c6f6 |
|---|
| Source note | uspto-grants-2013_01 |
|---|