HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717851Generated: October 25, 2026
Lithium Carbonate → 1-{2-Hydroxy-4-[3-(3-iodo-benzyl)-[1,2,4]oxadiazol-5-ylmethoxy]-3-methyl-phenyl}-ethanone
https://huagongshe.com/reaction/1717851
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Carbonate | HCID 11125 | — |
| Reactant | 3-(3-Amino-1,2,4-oxadiazol-5-yl)-1-azabicyclo(2.2.1)heptane | HCID 163938 | — |
| Reactant | 1-(2,4-Dihydroxy-3-methylphenyl)ethan-1-one | HCID 592139 | — |
| Reactant | 5-Chloromethyl-3-(3-iodo-benzyl)-[1,2,4]oxadiazole | HCID 57438412 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-{2-Hydroxy-4-[3-(3-iodo-benzyl)-[1,2,4]oxadiazol-5-ylmethoxy]-3-methyl-phenyl}-ethanone | HCID 66699621 | 53.8% |
Reaction Steps
Add lithium carbonate (49 mg, 0.66 mmol) and 5-chloromethyl-3-(3-iodo-benzyl)-[1,2,4]oxadiazole (200 mg, 0.60 mmol) to a solution of 1-(2,4-dihydroxy-3-methyl-phenyl)-ethanone (110 mg, 0.66 mmol) in anhydrous dimethylformamide (20 mL) 4]oxadiazole (200 mg, 0.60 mmol). Heat the reaction mixture at 60° C. overnight. Cool the reaction mixture to RT, pour into H2O, and extract with diethyl ether (3×). Combine the organic layers, wash with brine, dry over sodium sulfate, and concentrate to provide the title compound (150 mg). LC-MS (m/e): 463 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803938B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-477f1e9d8ca0420e8874bcbb37b678d0 |
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| Source note | uspto-grants-2010_09 |
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