HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 54414235, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 54417248 | HCID 54417248 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 54414235 | HCID 54414235 | 99% |
Reaction Steps
Acetic anhydride (36 mg) was added to a solution of (2R)-4-(2-aminoethanesulfonyl)-N-tert-butoxy-1-tert-butoxycarbonyl-2-piperazinecarboxamide (130 mg) in AcOH (2 ml). The reaction mixture was stirred at ambient temperature for 3 hours. The mixture was concentrated in vacuo, and the residue was partitioned between AcOEt and saturated aqueous NaHCO3 solution. The organic layer was washed with saturated aqueous NaCl solution, dried over MgSO4, and concentrated in vacuo to give 142 mg of (2R)-4-[2-(acetylamino)-ethanesulfonyl]-N-tert-butoxy-1-tert-butoxycarbonyl-2-piperazinecarboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06489324B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-c65dc1804e4b4a69b115274325ec3f14 |
| Source note | uspto-grants-2002_12 |