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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378366Generated: October 29, 2026

Piperidine → HCID 11033868, compound

https://huagongshe.com/reaction/1378366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantL-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
ProductHCID 11033868HCID 1103386880%

Reaction Steps

In substantially the same manner as Working Example 2, piperidine (0.86 g, manufactured by Wako Pure Chemical Industries, Ltd.).was condensed with Boc-L-leucine (2.74 g, manufactured by Peptide Institute, Inc.) to give N-(Boc-L-leucyl)piperidine (3.34 g) as white needles (yield 80%). The Boc group of the product was deprotected by using TFA, and 1.20 g of thus-deprotected compound was condensed, in substantially the same manner as Working Example 2, with (2S,3S)-ethyl hydrogen N-Z-aziridine-2,3-dicarboxylate (Compound 1, 1.93 g) to give the above-titled compound (Compound 23; 1.10 g) as a pale yellow oily product (yield 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668128
Source datasetuspto-grants-1997_09
ORD IDord-ab8a504b840f41b6adcfcfb1a7d90283
Source noteuspto-grants-1997_09