HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 54136579, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 57010773 | HCID 57010773 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54136579 | HCID 54136579 | 49.6% |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
To a solution of (2S,4R)-1-allyloxycarbonyl-2-(4-formyl-2-oxopiperazin-1-yl) methyl-4-(methanesulfonyloxy)pyrrolidine (14.2 g) in methanol (60 ml) was added conc. hydrochloric acid (12.2 ml) under ice cooling with stirring, and the mixture was stirred at the same temperature for 10 hours. The mixture was cooled to 5° C. and 28% sodium methoxidemethanol solution (28.2 ml) was added to it. The mixture was filtered, and the filtrate was evaporated in vacuo. To the residue was added chloroform. The mixture was dried over anhydrous magnesium sulfate and evaporated in vacuo to give (2S,4R)-1-allyloxycarbonyl-2-(2-oxopiperazin-1-yl) methyl-4-(methanesulfonyloxy)pyrrolidine (6.54 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05608056 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-17453d55002e410f908a9bf6e8235920 |
| Source note | uspto-grants-1997_03 |