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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | di-tert-butyl (2S)-2-(((3S)-3-methyl-4-morpholinyl)methyl)-1,4-piperazinedicarboxylate | HCID 66582706 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3S)-3-methyl-4-((2R)-2-piperazinylmethyl)morpholine trihydrochloride | HCID 66582623 | 107.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431563B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-699f67b155dd4dd09fed7cc07db7616d |
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| Source note | uspto-grants-2013_04 |
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