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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185483Generated: October 31, 2026

4-Methylmorpholine → 4-(3,5dichlorophenoxy)piperidine Dihydrochloride

https://huagongshe.com/reaction/2185483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactantn-Tert-butoxycarbonyl-trans-4-(n-tert-butoxycarbonylglycylamino)-d-prolineHCID 21341552—
Reactant4-(3,5-Dichlorophenoxy)piperidineHCID 22458412—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4-(3,5dichlorophenoxy)piperidine DihydrochlorideHCID 86758124347.7%

Reaction Steps

N-Methylmorpholine (70 μL) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (114 mg) were added to a solution of trans-4-(N-tert-butoxycarbonylglycylamino)-N-tert-butoxycarbonyl-D-proline (Compound D105 (F), 220 mg), 4-(3,5-dichlorophenoxy)piperidine (154 mg) and 1-hydroxybenzotriazole (85 mg) in tetrahydrofuran (8 mL) and N,N-dimethylformamide (2 mL) at room temperature. After stirring at room temperature for 12 hr, the reaction mixture was partitioned between ethyl acetate and 1 N hydrochloric acid. The organic layer was washed with saturated sodium hydrogen carbonate and brine. After drying over anhydrous sodium sulfate, the organic layer was evaporated in vacuo. The residue was washed with hexane to give the titled compound (347 mg) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399629B1
Source datasetuspto-grants-2002_06
ORD IDord-e4bd081705494bc1983af18eb476ca84
Source noteuspto-grants-2002_06