HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868815Generated: November 2, 2026
3-Tert-butyl-1,2-oxazol-5-amine → HCID 71295250, compound
https://huagongshe.com/reaction/868815
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Tert-butyl-1,2-oxazol-5-amine | HCID 2095694 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 71295370 | HCID 71295370 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 71295250 | HCID 71295250 | 46% |
Reaction Steps
100 mg of 5-(2-fluoropyridin-4-yl)-2-(tetrahydropyran-4-yloxy)benzonitrile are suspended in 6 ml of dioxane in a 50 ml three-necked flask under N2, 52 mg of 3-tert-butylisoxazol-5-ylamine and 79 mg of KOtBu are added. The yellow solution is stirred at 80° C. for 2.5 h. For work-up, the reaction mixture is evaporated in a rotary evaporator, the residue is taken up in ethyl acetate and water and extracted. The collected organic phases are dried, filtered and evaporated. The crude product is purified by preparative HPLC, giving the desired product in 46% yield; HPLC-MS Rt. [min] 2.556; HPLC-MS [M+H] 419;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969335B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-acc971eb0ceb44f498a70c234ff3969c |
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| Source note | uspto-grants-2015_03 |
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