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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489897Generated: October 30, 2026

Morpholine → HCID 7183045, compound

https://huagongshe.com/reaction/489897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
Reactant1-(1,1-Dimethylethyl) (3R)-1,3-piperidinedicarboxylateHCID 643516—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventDichloromethaneHCID 6344—
ProductHCID 7183045HCID 7183045—

Reaction Steps

(3R)-Piperidine-1,3-dicarboxylic acid 1-tert-butyl ester (2.64 g, 11.5 mmol), benzotriazo-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP, 1.1 eq., 5.61 g) and 1-hydroxybenzotriazole hydrate (0.1 eq., 180 mg) were dissolved in anhydrous dichloromethane (30 mL) under nitrogen and morpholine (1.1 eq., 1.11 mL) was added followed by triethylamine (3 eq., 4.82 mL). The solution briefly came to reflux and was then allowed to stir for 16 hr at ambient temperature. The solution was washed with 0.2M sodium hydroxide solution (×2), dried over anhydrous sodium sulfate and the solvent was removed under vacuum. The residue was dissolved in anhydrous toluene and the solvent again removed under vacuum. The product was purified by chromatography on silica gel eluting with a 5% to 10% methanol in dichloromethane gradient. The product was dissolved in ethyl acetate (30 mL), saturated with hydrogen chloride at −78° C. then stirred at room temperature for 1 hr. The solvent was evaporated in a stream of dry nitrogen. The solid residue was dissolved in water (˜5 mL) followed by sodium hydroxide (1 g). Xylene was added and the solvent was removed under vacuum. The residue was extracted with dichloromethane, the organic solution was filtered through Celite® and the solvent was evaporated under vacuum to give the title compound as a colorless oil which crystallized on refrigeration (2.25 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979741B2
Source datasetuspto-grants-2005_12
ORD IDord-240df4f512c24c5ca854d172fbcd5910
Source noteuspto-grants-2005_12