HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644642Generated: October 31, 2026
3-Isoxazolamine, 5-(1,1-dimethylethyl)- → HCID 25204104, compound
https://huagongshe.com/reaction/1644642
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Isoxazolamine, 5-(1,1-dimethylethyl)- | HCID 171473 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | 4-Iodo-N-(thiazol-2-yl)benzenesulfonamide | HCID 1019318 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 25204104 | HCID 25204104 | 1,478.4% |
Reaction Steps
To a mixture of 4-iodo-N-thiazol-2-yl-benzenesulfonamide (50 mg, 0.1 mmol, 1.0 equiv), tris(dibenzylideneacetone)dipalladium(0) (5 mg, 0.005 mmol, 0.04 equiv), 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (10 mg, 0.0016 mmol, 0.12 equiv) and 3-amino-5-tert-butylisoxazole (23 mg, 0.16 mmol, 1.2 equiv) in 1.8 mL of anhydrous 1,4-dioxane was added sodium tert-butoxide (39 mg, 0.41 mmol, 3.0 equiv). The vial was capped, and the reaction mixture was heated 30 min at 150° C. in the microwave. The crude reaction mixture was filtered through celite then concentrated in vacuo. The residue was taken up in chloroform-methanol, concentrated onto celite, and purified via automated flash chromatography (12 g SiO2, gradient from hexanes to ethyl acetate). The appropriate fractions were collected, concentrated in vacuo, then purified further via reverse phase HPLC. The solvent was removed by lyophilization to afford the product as a white solid (9 mg, 20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124610B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-12fcc208f79847769d4dd254cbc1958c |
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| Source note | uspto-grants-2012_02 |
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