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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydro-4H-pyran-4-one | HCID 121599 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (S)-Azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amide | HCID 67953683 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-1-(Tetrahydro-pyran-4-yl)-azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383615B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-8c09f9cb31b24669a451f1169a1a5fa9 |
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| Source note | uspto-grants-2013_02 |
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