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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389860Generated: November 1, 2026

Acetic Acid → (S)-1-(Tetrahydro-pyran-4-yl)-azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amide

https://huagongshe.com/reaction/389860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(S)-Azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amideHCID 67953683—
SolventDimethylformamideHCID 6228—
Product(S)-1-(Tetrahydro-pyran-4-yl)-azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amideHCID 49847677—

Reaction Steps

To a solution of (S)-Azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amide; hydrochloride (78.6 mg; 0.303 mol) in DMF (1 mL) is added tetrahydro-4H-pyran-4-one (0.056 mL; 0.606 mmol) and acetic acid (0.069 mL; 1.212 mmol). The reaction is stirred at room temperature for 50 minutes before adding sodium cyanoborohydride (57 mg; 0.909 mmol). The reaction mixture is left stifling at room temperature for 18 hours. After this time, the reaction mixture is quenched with saturated sodium bicarbonate aqueous solution and extracted with ethyl acetate twice. The organics are combined and washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography on silica gel using methanol/methylene chloride provides the title compound, m/z 308 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383615B2
Source datasetuspto-grants-2013_02
ORD IDord-8c09f9cb31b24669a451f1169a1a5fa9
Source noteuspto-grants-2013_02