HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972602Generated: November 1, 2026
Hydrochloric Acid → N-(2-methylpropyl)-N-((2R)-2-piperazinylmethyl)methanesulfonamide dihydrochloride
https://huagongshe.com/reaction/1972602
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | di-tert-butyl (2R)-2-(((2-methylpropyl)(methylsulfonyl)amino)methyl)-1,4-piperazinedicarboxylate | HCID 66582603 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2-methylpropyl)-N-((2R)-2-piperazinylmethyl)methanesulfonamide dihydrochloride | HCID 66582657 | 105% |
Reaction Steps
A 250-mL round-bottomed flask was charged with di-tert-butyl (2R)-2-(((2-methylpropyl)(methylsulfonyl)amino)methyl)-1,4-piperazinedicarboxylate (0.840 g, 1.87 mmol), HCl (4.0 M in 1,4-dioxane, 2.4 mL, 9.6 mmol, Sigma-Aldrich, St. Louis, Mo.) and EtOAc (20 mL). The reaction mixture was heated at 70° C. for 24 h and then was allowed to cool to room temperature. The resulting white solid was collected via filtration and washed with EtOAc to give N-(2-methylpropyl)-N-((2R)-2-piperazinylmethyl)methanesulfonamide dihydrochloride (0.633 g) as a white solid.
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-20c5f955cbe24006ac35f41a59ce4ad3 |
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| Source note | uspto-grants-2013_04 |
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