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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972590Generated: November 1, 2026

Hydrochloric Acid → (3S)-3-methyl-4-((2R)-2-piperazinylmethyl)morpholine trihydrochloride

https://huagongshe.com/reaction/1972590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantdi-tert-butyl (2S)-2-(((3S)-3-methyl-4-morpholinyl)methyl)-1,4-piperazinedicarboxylateHCID 66582706—
SolventEthyl AcetateHCID 8857—
Product(3S)-3-methyl-4-((2R)-2-piperazinylmethyl)morpholine trihydrochlorideHCID 66582623107.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

A 250-mL round-bottomed flask was charged with di-tert-butyl (2S)-2-(((3S)-3-methyl-4-morpholinyl)methyl)-1,4-piperazinedicarboxylate (2.46 g, 6.16 mmol, step 2), HCl (4.0 M solution in 1,4-dioxane, 4.62 mL, 18.5 mmol, Sigma-Aldrich, St. Louis, Mo.) and EtOAc (100 mL). The reaction mixture was heated at 70° C. for 3 h. At this time, additional HCl (4.0 M solution in 1,4-dioxane, 5.00 mL, 20.0 mmol) was added and heating at 70° C. was resumed for an additional 3 h. The reaction mixture was cooled to room temperature and the resulting white solid was collected, washed with EtOAc and dried overnight under reduced pressure to afford (3S)-3-methyl-4-((2R)-2-piperazinylmethyl)morpholine trihydrochloride (2.05 g) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-699f67b155dd4dd09fed7cc07db7616d
Source noteuspto-grants-2013_04