HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272700Generated: October 26, 2026
N-Hydroxyacetamidine → 5-(4-Iodo-2-methoxyphenyl)-3-methyl-1,2,4-oxadiazole
https://huagongshe.com/reaction/272700
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Hydroxyacetamidine | HCID 30926 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 4-Iodo-2-methoxybenzoic acid | HCID 13450756 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-Iodo-2-methoxyphenyl)-3-methyl-1,2,4-oxadiazole | HCID 69218487 | 39% |
Reaction Steps
A mixture of 4-iodo-2-methoxy benzoic acid (83 mg, 0.3 mmol), HATU (114 mg, 0.3 mmol), DIEA (26 μL, 0.15 mmol), and HOBt (8 mg, 0.06 mmol) in DMF was stirred at room temperature for 5 minutes. Acetamide oxime (22 mg, 0.3 mmol) was added, and reaction was stirred for 30 minutes at room temperature. The reaction was then heated to 110° C. for 16 hours. Cooled to room temperature. Partitioned between ethyl acetate and water. The organic layer was washed with brine, dried (MgSO4), filtered, and concentrated under vacuum. The residue was purified by HPLC to provide 37 mg (39%) of desired product. MS (ESI) m/e 317 (M+H)+, 1H NMR (300 MHz, DMSO-d6): □ 7.70 (d, J=8.14 Hz, 1H), 7.64 (d, J=1.36 Hz, 1H), 7.53 (dd, J=8.31-1.53 Hz, 1H), 3.94 (s, 3H), 2.40 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456169B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-4ce947c228d14b578fb09dc10cdefc76 |
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| Source note | uspto-grants-2008_11 |
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