HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634276Generated: October 30, 2026
3-(3-iodo-1-tosyl-1H-indol-5-yl)-1,2,4-oxadiazol-5-amine → 3-(3-(6-isopropoxypyridin-2-yl)-1-tosyl-1H-indol-5-yl)-1,2,4-oxadiazol-5-amine
https://huagongshe.com/reaction/634276
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(3-iodo-1-tosyl-1H-indol-5-yl)-1,2,4-oxadiazol-5-amine | HCID 68328482 | — |
| Reactant | 2-Isopropoxy-6-(tributylstannyl)pyridine | HCID 68328619 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3-(6-isopropoxypyridin-2-yl)-1-tosyl-1H-indol-5-yl)-1,2,4-oxadiazol-5-amine | HCID 68328799 | 61.6% |
Reaction Steps
Argon gas was bubbled through a solution of 3-(3-iodo-1-tosyl-1H-indol-5-yl)-1,2,4-oxadiazol-5-amine (350 mg, 0.73 mmol) and 2-isopropoxy-6-(tributylstannyl)pyridine (374 mg, 0.87 mmol) in dry DMF (3.5 mL) for 15 min. To the mixture was added CuI (139 mg, 0.73 mmol) and Pd(PPh3)4 (84 mg, 0.073 mmol) and argon gas was further bubbled for additional 15 min. The reaction was heated at 90° C. for 1 h then cooled to RT. The reaction was quenched with ice cold water. The resulting suspension was filtered and washed with water. The solid was purified with basic alumina column chromatography (eluent: 20% EtOAc in petroleum ether) to give 3-(3-(6-isopropoxypyridin-2-yl)-1-tosyl-1H-indol-5-yl)-1,2,4-oxadiazol-5-amine (220 mg, 61.5%). MS (ESI, pos. ion) m/z: 490.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321756B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-41491c47786a45ccbffe909b66696de5 |
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| Source note | uspto-grants-2016_04 |
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