HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(pyrrolidin-2-yl)acetate → N--BOC-L-lysyl-(S)-2-pyrrolidineacetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(pyrrolidin-2-yl)acetate | HCID 336545 | — |
| Reactant | epsilon-tert-Butyloxycarbonyl-lysine | HCID 2733284 | — |
| Product | N--BOC-L-lysyl-(S)-2-pyrrolidineacetic acid ethyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634716 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-8419f80b7dd44c5daf578aa5c26a443c |
| Source note | uspto-grants-1987_01 |