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HCID 10755519, 화합물 → HCID 10657826, 화합물

HRID 1957773
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HRID 1957773 반응식
C([NH:4][CH:5]([CH2:9][C:10]([C:12]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:13]=1[NH2:19])=[O:11])[C:6]([OH:8])=[O:7])(=O)C>Cl>[NH2:4][C@H:5]([CH2:9][C:10]([C:12]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:13]=1[NH2:19])=[O:11])[C:6]([OH:8])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 10755519HCID 10755519, 화합물

생성물 1

HCID 10657826HCID 10657826, 화합물수율 61.7%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A solution of (-)-2-acetamido-4-(2-amino-5-chlorophenyl)-4-oxo-butyric acid (0.76 g, 2.67 mmol) in 2N HCl (90 ml) was heated at reflux temperature for 3 h. The aqueous solution was evaporated to dryness, the residue was dissolved in water, washed with CH2Cl2 and evaporated again. The residue was dissolved in water (30 ml) and adjusted to pH 6.5 with 1N NaOH: a light yellow solid separated. The solid was filtered and washed with cold water to obtain (R)-(+)-2-amino-4-(2-amino-5-chlorophenyl)-4-oxo-butyric acid (0.40 g; 59.7%; m.p. 210°-211° C. (dec.); [α]20D =+11.5 (1%, CH3COOH); ee=96%).

후처리

  1. temperatureat reflux temperature for 3 h
custom
The aqueous solution was evaporated to dryness
  • dissolutionthe residue was dissolved in water
  • washwashed with CH2Cl2
  • customevaporated again
  • dissolutionThe residue was dissolved in water (30 ml)
  • customa light yellow solid separated
  • filtrationThe solid was filtered
  • washwashed with cold water
  • 출처 및 근거

    ORD 기록
    ord-57918b16e5ce4c5aac1e51aa3b6d04f1
    출처 데이터셋
    uspto-grants-1998_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05786508

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