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Hydrochloric Acid → HCID 69820402, 화합물

HRID 1840523
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HRID 1840523 반응식
[OH-].[Li+].[NH2:3][C:4]1[N:5]=[CH:6][C:7]([CH2:10][CH2:11][CH2:12][C@H:13]([NH:18][C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[C:14]([O:16]C)=[O:15])=[N:8][CH:9]=1.Cl>CO.O>[NH2:3][C:4]1[N:5]=[CH:6][C:7]([CH2:10][CH2:11][CH2:12][C@H:13]([NH:18][C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[C:14]([OH:16])=[O:15])=[N:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 86590135HCID 86590135, 화합물

생성물 1

HCID 69820402HCID 69820402, 화합물수율 97%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

Lithium hydroxide (1.2 g, 28.6 mmol) is added, at 0° C., to a solution of methyl (S)-5-(5-amino-2-pyrazinyl)-2-[[(1,1-dimethylethoxy)carbonyl]amino]pentanoate (7.75 g, 23.9 mmol) in methanol (60 ml) and water (20 ml). The mixture is allowed to warm to room temperature and stirring is continued for 18 hours. The methanol is evaporated off under reduced pressure and the residue obtained is cooled to 0° C., acidified to pH 3-4 with 1N hydrochloric acid (30 ml), extracted with ethyl acetate (2×200 ml), washed with brine (50 ml), dried over sodium sulphate, filtered and concentrated under reduced pressure. 7.17 g of (S)-5-(5-amino-2-pyrazinyl)-2-[[(1,1-dimethylethoxy)carbonyl]amino]pentanoic acid are obtained in the form of a white powder, which is used without further purification in the following step.

후처리

  1. customThe methanol is evaporated off under reduced pressure
  2. customthe residue obtained
  3. temperatureis cooled to 0° C.
  4. extractionextracted with ethyl acetate (2×200 ml)
  5. washwashed with brine (50 ml)
  6. dry with materialdried over sodium sulphate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-03d9dab340a740b1b7054d10f7dba114
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06680329B2

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