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Stannous Chloride → 6-Amino-7-chloro-1,4-dihydro-2,3-quinoxalinedione

HRID 439476
ノート
印刷プレビュー

反応式

HRID 439476 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][C:13]=1[Cl:14])[NH:10][C:9](=[O:15])[C:8](=[O:16])[NH:7]2)([O-])=O.Cl[Sn]Cl>C(O)C>[NH2:1][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][C:13]=1[Cl:14])[NH:10][C:9](=[O:15])[C:8](=[O:16])[NH:7]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24479Stannous ChlorideHCID 106101506-Chloro-7-nitro-quinoxaline-2,3-diol

生成物 1

HCID 144236496-Amino-7-chloro-1,4-dihydro-2,3-quinoxalinedione収率 45.6%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
90 °C

実験手順

To a stirred mixture of 6-nitro-7-chloro-1,4-dihydro-2,3-quinoxalinedione (35 mg, 0.145 mMol) in ethanol (2 mL) was added SnCl2 ·2H2O (163 mg, 0.724 mMol) in one portion. The mixture was refluxed at 80° C. (oil bath 90° C.) with stirring for 0.5 h to form a clear solution and continually refluxed for another 0.5 h. It was then cooled to room temperature and the yellow precipitate was collected by filtration, followed by washing with cold ethanol (1×1 mL) to give 25 mg (82%) of crude title compound (contains minor impurities by NMR). Crystallization from DMSO/H2O gave 14 mg of pure title compound as bright yellow needles, mp:>350° C. (dec. from 335° C.). IR (KBr, cm-1): 3406, 3356, 3212, 1668, 1637, 1518, 1437. NMR (1H, DMSO-d6): d 5.306 (s, 2H); 6.551 (s, 1H); 6.940 (s, 1H); 11.606 (s, 1H); 11.788 (s, 1H). HRMS: calcd for C8H6N3O2Cl (M+) m/z: 211.0147; found 211.0159. Potency relative to DCK: 28.0%.

後処理

  1. customto form a clear solution
  2. temperaturecontinually refluxed for another 0.5 h
  3. temperatureIt was then cooled to room temperature
  4. filtrationthe yellow precipitate was collected by filtration
  5. washby washing with cold ethanol (1×1 mL)
  6. customto give 25 mg (82%) of crude title compound (contains minor impurities by NMR)
  7. customCrystallization from DMSO/H2O

出典と根拠

ORDレコード
ord-6a6e71ff48cf41869abd53090333aa30
出典データセット
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05514680

反応ノート

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