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Dinitrofluorobenzene → 3-(2-Aminobenzoyl)-2-(2,4-dinitroanilino)propanoic acid

HRID 1877343
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HRID 1877343 반응식
[CH:1]1[CH:2]=[CH:3][C:4]([NH2:15])=[C:5]([C:7]([CH2:9][C@H:10]([NH2:14])[C:11]([OH:13])=[O:12])=[O:8])[CH:6]=1.[N+:16]([C:19]1[CH:24]=[C:23]([N+:25]([O-:27])=[O:26])[CH:22]=[CH:21][C:20]=1F)([O-:18])=[O:17].C([O-])(O)=O.[Na+]>C(O)C>[NH2:15][C:4]1[CH:3]=[CH:2][CH:1]=[CH:6][C:5]=1[C:7]([CH2:9][CH:10]([NH:14][C:20]1[CH:21]=[CH:22][C:23]([N+:25]([O-:27])=[O:26])=[CH:24][C:19]=1[N+:16]([O-:18])=[O:17])[C:11]([OH:13])=[O:12])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6264DinitrofluorobenzeneHCID 161166KynurenineHCID 516892Sodium Bicarbonate

생성물 1

HCID 112802543-(2-Aminobenzoyl)-2-(2,4-dinitroanilino)propanoic acid수율 71%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

L-Kynurenine (125 mg) is dissolved in 5 cc of absolute ethanol in a 50 cc flask. A solution of 2,4-dinitrofluorobenzene, 71 mg in EtOH 5 cc is then added (a clear yellow solution is formed). After five minutes, 2 cc of a 10% NaHCO3 solution are introduced drop-wise in the flask. The reaction is left at room temperature overnight. The following morning the formed light yellow precipitate is filtered, washed with water and ethanol and dried in UHV obtaining 80 mg of product (approx. yield 71%).

후처리

  1. customis formed)
  2. waitThe reaction is left at room temperature overnight
  3. filtrationThe following morning the formed light yellow precipitate is filtered
  4. washwashed with water and ethanol
  5. customdried in UHV

출처 및 근거

ORD 기록
ord-4ae749a44c1b47d488d85366baef0a30
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08309767B2

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