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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389862Generated: October 31, 2026

Hydrochloric Acid → (S)-1-(1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl)-azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amide

https://huagongshe.com/reaction/389862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl chlorideHCID 21694907—
Reactant(S)-Azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amideHCID 67953683—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(S)-1-(1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl)-azetidine-2-carboxylic acid (3-tert-butyl-isoxazol-5-yl)-amideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383615B2
Source datasetuspto-grants-2013_02
ORD IDord-80d219973ece4c0cadc9da456b7f3b87
Source noteuspto-grants-2013_02