반응 #2006452

ord-1312f71c753a4459809e1a841e31ad84

반응 방정식

CC(C)(C)OC(=O)N1CCCC(=O)C1
N-Boc-3-piperidinone
O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
D-glucose
C[C@H](N)C(=O)O
L-alanine
Cc1ncc(COP(=O)(O)O)c(C=O)c1O
pyridoxal phosphate
CC(C)(C)OC(=O)N1CCCC(=O)C1
N-Boc-3-piperidinone
O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
D-glucose
Cc1ncc(COP(=O)(O)O)c(C=O)c1O
pyridoxal phosphate
CC(C)(C)OC(=O)N1CCCC(N)C1
N-Boc-3-aminopiperidine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwere added
  2. 2
    workup.ADDITIONwere added
  3. 3
    기타During the reaction
  4. 4
    기타the reaction liquid
  5. 5
    workup.ALIQUOTwas sampled
  6. 6
    추출From the sample, N-Boc-3-aminopiperidine was extracted by the addition of ethyl acetate

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08168412B2uspto-grants-2012_05