HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559574Generated: October 29, 2026
Water → (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanamine
https://huagongshe.com/reaction/559574
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanol | HCID 66974146 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanamine | HCID 66974227 | 68.7% |
Reaction Steps
To a suspension of (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanol (0.39 g, 1.23 mmol) in CH3CN (7 mL), SOCl2 (2.5 mL) was added. Upon the addition, the suspension became clear. It was then concentrated in vacuo. The residue was dissolved in DMF (7 mL), NaN3 (0.32 g, 4.92 mmol) was added. The mixture was stirred at room temperature overnight. H2O and EtOAc were added. The organic phase was separated, washed with 5% NaHCO3, dried over Na2SO4, concentrated in vacuo. The residue was dissolved in MeOH (6 mL), Ra—Ni (50% slurry in H2O, ˜200 mg) was added. The mixture was hydrogenated under balloon H2 for 2 h. It was then filtered through celite. The filtrate was concentrated in vacuo to give (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanamine as a solid (0.268 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063077B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-61abd0b672844a729a9737df354dd523 |
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| Source note | uspto-grants-2011_11 |
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