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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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dimethyl 3-methyl-L-aspartate → (2S)-2-amino-4-methoxy-3-methyl-4-oxobutanoic acid

HRID 1424213
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HRID 1424213 반응식
[CH3:1][CH:2]([C:9]([O:11][CH3:12])=[O:10])[C@@H:3]([C:5]([O:7]C)=[O:6])[NH2:4].[NH4+]=S>O.C([O-])([O-])=O.O.O.[Cu].[Cu+2]>[NH2:4][C@@H:3]([CH:2]([CH3:1])[C:9]([O:11][CH3:12])=[O:10])[C:5]([OH:7])=[O:6]
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참가 물질

4

반응물 1

HCID 86699126dimethyl 3-methyl-L-aspartate

생성물 1

HCID 86699124(2S)-2-amino-4-methoxy-3-methyl-4-oxobutanoic acid

시약·촉매·용매 2

HCID 10922056HCID 10922056, 화합물촉매HCID 962Water용매

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온도
70 °C

실험 절차

A mixture of dimethyl 3-methyl-L-aspartate (Preparation 64, 23 g, 82.55 mmol), CuCO3.Cu(OH)2 (21.9 g, 99.05 mmol) in water (250 mL) was heated to 70° C. for 4 hours. The resulting precipitate was filtered and the filtrate cooled to 0° C. Ammonium sulfide (20% in water, 67.5 mL, 198 mmol) was added slowly ensuring the temperature did not rise above 5° C. The reaction was filtered through arbocel to remove the copper residues and the filtrate concentrated in vacuo. The residue was redissolved in MeOH and filtered through arbocel, with concentration of the filtrate to dryness to afford the title compound as an oil that was used directly in the next step.

후처리

  1. filtrationThe resulting precipitate was filtered
  2. temperaturethe filtrate cooled to 0° C
  3. customdid not rise above 5° C
  4. filtrationThe reaction was filtered through arbocel
  5. customto remove the copper residues
  6. concentrationthe filtrate concentrated in vacuo
  7. dissolutionThe residue was redissolved in MeOH
  8. filtrationfiltered through arbocel, with concentration of the filtrate to dryness

출처 및 근거

ORD 기록
ord-aa131b17a9a447f68494f857fa7965ea
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927587B2

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