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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296671Generated: November 1, 2026

Acetic Anhydride → HCID 54414235, compound

https://huagongshe.com/reaction/2296671

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 numberUS06489324B2
Source datasetuspto-grants-2002_12
ORD IDord-c65dc1804e4b4a69b115274325ec3f14
Source noteuspto-grants-2002_12