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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336180Generated: October 30, 2026

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

https://huagongshe.com/reaction/336180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl chlorideHCID 21694907—
ReactantPiperidine-3-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amideHCID 58563805—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl)-piperidine-3-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amideHCID 46872044—

Reaction Steps

To a solution of piperidine-3-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide; hydrochloride (100 mg; 0.347 mmol) in anhydrous THF (1 mL) is added triethylamine (0.098 mL; 0.7 mmol) and 1,1-dioxo-1λ6-thiomorpholine-4-carbonyl chloride (71.15 mg; 0.36 mmol). The reaction mixture is left stirring at room temperature overnight. The reaction mixture is diluted with water and extracted with ethyl acetate 3 times. The organics are combined and washed with brine, dried over Na2SO4, filtered and concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889670B2
Source datasetuspto-grants-2014_11
ORD IDord-17bba68d3261432b941d55a2e4b12c1a
Source noteuspto-grants-2014_11