반응 #2006453

ord-0d44b2af5d6a4911b01d20c5c4d4e38e

반응 방정식

[Na+].[OH-]
sodium hydroxide
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
NC(=O)c1ccc[n+]([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)c1
NAD+
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)N1CCCCC1N
N-Boc-aminopiperidine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타(pNTPSPAG), obtained in Example 10, which
  2. 2
    workup.ADDITIONwas added so that total volume was 30 ml

실험 절차

To a flask containing 0.6 g of a substrate N-Boc-3-piperidinone, 0.82 g of D-glucose, 4 mg of NAD+, 1.62 g of L-alanine, and 4.0 mg of pyridoxal phosphate, a culture fluid of the recombinant E. coli HB101 (pNTPSPAG), obtained in Example 10, which expresses TPS, PALDH, and GDH was added so that total volume was 30 ml. The resultant product was stirred at 30° C. for 20 hours while being adjusted to a pH of 6.8 by drippage of 5 N aqueous solution of sodium hydroxide. The amount of N-Boc-aminopiperidine produced and the optical purity thereof were measured according to the method described in Example 19. In the result, the amount produced was 0.54 g. The absolute configuration of N-Boc-aminopiperidine was (S), and the optical purity was 99.4% e.e.

출처

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