HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → methyl 2-(R)-[(piperazine-1-sulfonyl)amino]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (R)-methyl 2-amino-3-methylbutanoate | HCID 2305648 | — |
| Reactant | methyl 2-(R)-[(4-tert-butoxycarbonylpiperazine-1-sulfonyl)amino]propionate | HCID 18727245 | — |
| Solvent | Dioxane methylene chloride | HCID 18626912 | — |
| Product | methyl 2-(R)-[(piperazine-1-sulfonyl)amino]propionate | HCID 18727249 | 91% |
Reaction Steps
Hydrogen chloride gas was bubbled through a solution of methyl 2-(R)-[(4-tert-butoxycarbonylpiperazine-1-sulfonyl)amino]propionate (3.6 g, 10.7 mmol) [prepared by proceeding as described in Example 2, but substituting 4-(5-chloropyridin-2-yloxy)piperidine and D-valine methyl ester with 1-tert-butoxycarbonyl-1,4-piperazine and D-alamine methyl ester, respectively] in 10% dioxane/methylene chloride (100 ml) for 10 min. The reaction was stirred at RT for 4 h and concentrated in vacuo to give methyl 2-(R)-[(piperazine-1-sulfonyl) amino]propionate (91%) as a white solid that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06130220 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-a2c49267a6cb41a5ae6b868b21c684b1 |
| Source note | uspto-grants-2000_10 |