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Dihydroxyacetone Phosphate → 6-azido-6-deoxy-D-xylo-hexulose

HRID 234707
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HRID 234707 반응식
[CH2:1]([OH:10])[C:2]([CH2:4][O:5]P(O)(O)=O)=[O:3].[N:11]([CH2:14][C@@H:15]([OH:18])[CH:16]=[O:17])=[N+:12]=[N-:13].[OH-].[Na+].CO>C(O)C(N)(CO)CO>[N:11]([CH2:14][C@@H:15]([OH:18])[C@H:16]([OH:17])[C@@H:1]([OH:10])[C:2](=[O:3])[CH2:4][OH:5])=[N+:12]=[N-:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 668Dihydroxyacetone PhosphateHCID 887MethanolHCID 14798Sodium HydroxideHCID 14110600(R)-3-azido-2-hydroxypropanal

생성물 1

HCID 228497576-azido-6-deoxy-D-xylo-hexulose수율 30%

시약·촉매·용매 1

HCID 6503Tris(hydroxymethyl)aminomethane
용매

실험 절차

DHAP (0.5 mmole) was added to an aqueous solution of (R)-3-azido-2-hydroxypropanal (1 mmole in 40 ml) and the pH value adjusted to 7.0 with 10N NaOH. To this solution was added fuculose-1-phosphate aldolase from E. coli (4 g), which had been treated with egg white lysozyme (40 mg) in Tris buffer (pH 7.5, 25 ml) for 1 hour at 35° C., to form a mixture and the mixture stirred slowly for 2 days. The stirred mixture was adjusted to a pH value of 4.7, and acid phosphatase (400 units) added. The resulting mixture was incubated at 37° C. for 48 hours, neutralized to a pH value of 7.0 and lyophilized. The residue was treated with MeOH and filtered to remove the insoluble material. The MeOH was removed under reduced pressure and the crude product purified with silica gel column chromatography (CHCl3 :MeOH=6:1) to give 6-azido-6-deoxy-D-xylo-hexulose in 30% yield.

후처리

  1. customto form a mixture
  2. additionadded
  3. waitThe resulting mixture was incubated at 37° C. for 48 hours
  4. filtrationfiltered
  5. customto remove the insoluble material
  6. customThe MeOH was removed under reduced pressure
  7. customthe crude product purified with silica gel column chromatography (CHCl3 :MeOH=6:1)

출처 및 근거

ORD 기록
ord-ef1c8fad648d4be8887303d4ee129858
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05596005

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