HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (S)-1-(1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl)-azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl chloride | HCID 21694907 | — |
| Reactant | (S)-Azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amide | HCID 67953683 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-1-(1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl)-azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amide | HCID 49847682 | — |
Reaction Steps
1,1-Dioxo-1λ6-thiomorpholine-4-carbonyl chloride (51.4 mg; 0.26 mmol) is added to a mixture of (S)-Azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amide; hydrochloride (69 mg; 0.265 mmol) and N,N-diisopropylethylamine (0.141 mL; 0.81 mmol) in THF (2 mL). The reaction mixture is stirred at room temperature for 2 hours. After this time, the reaction mixture is diluted with dichloromethane and washed with water. The layers are separated and the aqueous layer is extracted with dichloromethane once. 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 385 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383615B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-80d219973ece4c0cadc9da456b7f3b87 |
| Source note | uspto-grants-2013_02 |