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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979837Generated: October 30, 2026

Ethyl 2-(pyrrolidin-2-yl)acetate → N--BOC-L-lysyl-(S)-2-pyrrolidineacetic acid ethyl ester

https://huagongshe.com/reaction/979837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(pyrrolidin-2-yl)acetateHCID 336545—
Reactantepsilon-tert-Butyloxycarbonyl-lysineHCID 2733284—
ProductN--BOC-L-lysyl-(S)-2-pyrrolidineacetic acid ethyl esterHCID 53706975—

Reaction Steps

N-α-CBZ, N- -BOC-L-lysine and ethyl-2-pyrrolidineacetate are condensed by the procedure of Example 1, Step C to give N-α-CBZ, N- -BOC-L-lysyl-(S)-2-pyrrolidine acetic acid ethyl ester. The N-α-CBZ group is removed by hydrogenolysis in ethanol containing one equivalent of acetic acid over 10% palladium on charcoal utilizing the procedure of P. G. Katsoyannis and G. P. Schwartz, Methods in Enzymology, 47, 546 (1974), to give N- -BOC-L-lysyl-(S)-2-pyrrolidineacetic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04634716
Source datasetuspto-grants-1987_01
ORD IDord-8419f80b7dd44c5daf578aa5c26a443c
Source noteuspto-grants-1987_01