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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908650Generated: October 27, 2026

4-tert-Butyl hydrogen N-((phenylmethoxy)carbonyl)-L-aspartate → 4-((S)-2-benzyloxycarbonylamino-3-tert-butoxycarbonyl-propionyl)-piperazine-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1908650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-Butyl hydrogen N-((phenylmethoxy)carbonyl)-L-aspartateHCID 111082—
ReactantO-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733286—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-((S)-2-benzyloxycarbonylamino-3-tert-butoxycarbonyl-propionyl)-piperazine-1-carboxylic acid ethyl esterHCID 66920269—

Reaction Steps

To a solution of 15.4 g (S)-2-Benzyloxycarbonylamino-succinic acid 4-tert-butyl ester, 24.4 ml NEM and 15.6 g TOTU in 80 ml DMF 7.5 g piperazine-1-carboxylic acid ethyl ester were added at RT and stirred for 16 h. The reaction mixture was then diluted with ethyl acetate and washed with aqueous LiCl (4 w/w) and saturated aqueous sodium hydrogen carbonate. The organic phase was dried over MgSO4 and the solvents were removed under reduced pressure. The crude product was used in the subsequent reaction. Yield: 23.0 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598179B2
Source datasetuspto-grants-2013_12
ORD IDord-390c5f15dc7441ce99ae0e6296d58905
Source noteuspto-grants-2013_12