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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Tert-butyl-1,2-oxazol-5-amineHCID 2095694—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 71295370HCID 71295370—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71295250HCID 7129525046%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969335B2
Source datasetuspto-grants-2015_03
ORD IDord-acc971eb0ceb44f498a70c234ff3969c
Source noteuspto-grants-2015_03