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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919270Generated: October 31, 2026

Pyridoxal 5'-phosphate → 1-BOC-3-Aminopiperidine

https://huagongshe.com/reaction/1919270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridoxal 5'-phosphateHCID 1051—
ReactantL-AlanineHCID 5950—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantTert-butyl 3-oxopiperidine-1-carboxylateHCID 2756825—
Product1-BOC-3-AminopiperidineHCID 545809—

Reaction Steps

After two hours in reaction, 1.25 g of N-Boc-3-piperidinone, 1.7 g of D-glucose, 1.0 g of L-alanine, and 3.3 mg of pyridoxal phosphate were added. Further, after five hours in reaction, 1.25 g of N-Boc-3-piperidinone, 1.7 g of D-glucose, and 3.3 mg of pyridoxal phosphate were added. During the reaction, the reaction liquid was sampled. From the sample, N-Boc-3-aminopiperidine was extracted by the addition of ethyl acetate after basifying the sample with 6 N aqueous solution of sodium hydroxide. The amount of N-Boc-3-aminopiperidine produced was measured by analyzing N-Boc-3-aminopiperidine under the following GC conditions. Further, by the law of the art, N-Boc-3-aminopiperidine thus obtained was acted on by 3,5-dinitrobenzyl chloride to form a dinitrobenzyl derivative. After that, the dinitrobenzyl derivative was analyzed under the following HPLC conditions, whereby the optical purity thereof was measured. In the result, the amount of N-Boc-3-aminopyrrolidine produced after 23.5 hours in reaction was 3.13 g. The absolute configuration of N-Boc-3-aminopyrrolidine was (S), and the optical purity was not less than 99.9% e.e.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168412B2
Source datasetuspto-grants-2012_05
ORD IDord-1312f71c753a4459809e1a841e31ad84
Source noteuspto-grants-2012_05