HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724221Generated: October 27, 2026
Ammonium Chloride → 7-(4'-Fluoro[1,1'-biphenyl]-3-yl)-6,7-dihydro-5h-pyrrolo[1,2-c]imidazol-7-ol
https://huagongshe.com/reaction/724221
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Bromo-4'-fluorobiphenyl | HCID 2756977 | — |
| Reactant | 5,6-Dihydropyrrolo[1,2-c]imidazol-7-one | HCID 11170960 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 7-(4'-Fluoro[1,1'-biphenyl]-3-yl)-6,7-dihydro-5h-pyrrolo[1,2-c]imidazol-7-ol | HCID 9796140 | 45.1% |
Reaction Steps
A solution (1.6 M; 1.98 ml) of n-butyl lithium in hexane was gently added dropwise to a solution of 3-bromo-4′-fluoro-1,1′-biphenyl (753 mg) in THF (10 ml) at −78° C., and the mixture was stirred at −78° C. for 30 min. A solution of 5,6-dihydro-7Hpyrrolo[1,2-c]imidazol-7-one (244 mg) in THF (10 ml) solution was gently added dropwise and the mixture was stirred at −78° C. for 1 h. A saturated aqueous ammonium chloride solution was added to the reaction mixture and the mixture was extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent, ethyl acetate→ethyl acetate:methanol=5:1) and recrystallized from acetone-hexane to give the title compound (265 mg) as colorless needle crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141598B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-6d5d550a3d10474193688d5d4178dcce |
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| Source note | uspto-grants-2006_11 |
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