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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2,5-Diamino-2-methylpentanoic acid hydrochloride → 2-Amino-5-[[1-(hydroxyimino)ethyl]amino]-2-methylpentanoic Acid, Dihydrochloride

HRID 1533175
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HRID 1533175 반응식
[ClH:1].[CH3:2][C:3]([C:9]([OH:11])=[O:10])([CH2:5][CH2:6][CH2:7][NH2:8])[NH2:4].[Cl:12][CH2:13][CH:14]=[N:15][OH:16]>O>[ClH:12].[ClH:1].[NH2:4][C:3]([CH3:2])([CH2:5][CH2:6][CH2:7][NH:8][C:14](=[N:15][OH:16])[CH3:13])[C:9]([OH:11])=[O:10]
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참가 물질

4

반응물 2

HCID 185191242,5-Diamino-2-methylpentanoic acid hydrochlorideHCID 57350373N-(2-Chloroethylidene)hydroxylamine

생성물 1

HCID 1784657012-Amino-5-[[1-(hydroxyimino)ethyl]amino]-2-methylpentanoic Acid, Dihydrochloride

시약·촉매·용매 1

HCID 962Water용매

실험 절차

α-Methyl-D,L-ornithine hydrochloride is protected as a copper complex via reaction with cupric carbonate in water at reflux. This protected amino acid is then reacted with chloroacetaldoxime as in Example 1. The product is eluted from Dowex with 1N ammonium hydroxide. Concentration in vacuo, followed by acidification with hydrochloric acid affords the title compound.

후처리

  1. temperatureat reflux
  2. washThe product is eluted from Dowex with 1N ammonium hydroxide
  3. concentrationConcentration in vacuo

출처 및 근거

ORD 기록
ord-40d2cece45814e91a657e2591a0b30bd
출처 데이터셋
uspto-grants-2001_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06207708B1

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