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Sodium Hydroxide → 4-Pyridylcarbamoyl-beta-alanine

HRID 358556
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HRID 358556 반응식
C([O:3][C:4](=[O:17])[CH2:5][CH2:6][NH:7][C:8](=[O:16])[NH:9][C:10]1[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=1)C.[OH-].[Na+]>CO.O>[N:13]1[CH:14]=[CH:15][C:10]([NH:9][C:8]([NH:7][CH2:6][CH2:5][C:4]([OH:17])=[O:3])=[O:16])=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 200664534-Pyridylcarbamoyl-beta-alanine ethyl ester

생성물 1

HCID 200664464-Pyridylcarbamoyl-beta-alanine수율 95%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

A solution of 2 g (8.4 mmol) of 4-pyridylcarbamoyl-beta-alanine ethyl ester and 0.37 g (9.2 mmol) of sodium hydroxide in 50 ml of methanol and 0.1 ml of water is kept agitated for 24 hr at room temperature. After concentration to dryness, the resulting oily residue is taken up in 15 ml of water. After washing with 3 x 10 ml of dichloromethane, the aqueous phase is acidified with a 3 N hydrochloric acid solution until a pH close to 3 is obtained. The precipitate formed is filtered, washed with 10 ml of cold water and then dried 1.36 g (yield 95%) of 4-pyridylcarbamoyl-beta-alanine is obtained in the form of a solid having a melting point of 222° C.

후처리

  1. concentrationAfter concentration to dryness
  2. washAfter washing with 3 x 10 ml of dichloromethane
  3. customa pH close to 3
  4. customis obtained
  5. customThe precipitate formed
  6. filtrationis filtered
  7. washwashed with 10 ml of cold water

출처 및 근거

ORD 기록
ord-36809863936945b4b1bcdb47ddd8771b
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04997667

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