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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271023Generated: November 2, 2026

Acetic Anhydride → HCID 54414235, compound

https://huagongshe.com/reaction/2271023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 54417248HCID 54417248—
SolventAcetic AcidHCID 176—
ProductHCID 54414235HCID 5441423599%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333324B1
Source datasetuspto-grants-2001_12
ORD IDord-b8bcde6cd6d34a2b85c2468b4b32b598
Source noteuspto-grants-2001_12