HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080313Generated: October 30, 2026
Potassium Carbonate → 1,1-Dimethylethyl 4-[(3'-cyano-3-biphenylyl)methyl]-1-piperazinecarboxylate
https://huagongshe.com/reaction/2080313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromobenzonitrile | HCID 23381 | — |
| Reactant | (3-((4-(Tert-butoxycarbonyl)piperazin-1-yl)methyl)phenyl)boronic acid | HCID 42609723 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | 1,1-Dimethylethyl 4-[(3'-cyano-3-biphenylyl)methyl]-1-piperazinecarboxylate | HCID 57736697 | 77.5% |
Reaction Steps
A mixture of {3-[(4-{[(1,1-dimethylethyl)oxy]carbonyl}-1-piperazinyl)methyl]phenyl}boronic acid (1 g), 3-bromobenzonitrile (0.56 g), potassium carbonate (1.725 g) and tetrakis triphenylphosphine palladium (180 mg) in dioxan/water (3:1, 4 mL) was sealed in a tube and heated at 150° C. for 15 minutes in a microwave vessel. After cooling to room temperature, the reaction mixture was then diluted with water (25 mL) and extracted with ethyl acetate (2×25 mL). The combined organic phases were dried (MgSO4) and concentrated under vacuum. The resulting crude residue was further purified by flash column chromatography on silica (100 g) to give the title compound (0.9 g) (purity ca 75%). LC/MS: m/z, 378 (M+H), 2.57 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932247B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-60c3438f7365416183980186927cfd73 |
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| Source note | uspto-grants-2011_04 |
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