反応 #3213

ord-454fe2e70f3f4c0c89014e75840e632f

反応方程式

COC(=O)c1nc2ccccc2c(N)c1C(=O)OC
dimethyl 4-aminoquinoline-2,3-dicarboxylate
NN.O
hydrazine hydrate
Nc1c2ccccc2nc2c(=O)[nH][nH]c(=O)c12
title compound
収率 98.8%
Nc1c2ccccc2nc2c(=O)[nH][nH]c(=O)c12
10-Amino-2,3-dihydropyridazino[4,5-b]quinoline-1,4-dione
収率 98.8%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度the resulting solution was refluxed for 3 hr
  2. 2
    ろ過filtered
  3. 3
    その他to separate the yellow precipitate (0.12 g)
  4. 4
    温度in refluxing acetic acid (4.5 mL) for 1 hr
  5. 5
    温度After cooling to room temperature the reaction mixture
  6. 6
    ろ過was filtered
  7. 7
    洗浄the collected solids washed with acetic acid and ethyl acetate
  8. 8
    その他Air drying

実験手順

To a stirred solution of dimethyl 4-aminoquinoline-2,3-dicarboxylate (0.15 g, 0.58 mM) in ethanol (4 mL) was added hydrazine hydrate (1.46 g, 29.2 mM) and the resulting solution was refluxed for 3 hr. The reaction mixture was cooled to room temperature and filtered to separate the yellow precipitate (0.12 g). This material was stirred in refluxing acetic acid (4.5 mL) for 1 hr. After cooling to room temperature the reaction mixture was filtered and the collected solids washed with acetic acid and ethyl acetate. Air drying provided the title compound (0.13 g, 68%) as an orange solid, mp>400° C.; MS(CI): 229 (M+H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05733910uspto-grants-1998_03