Hydrochloric Acid → HCID 68412119, compound

HRID 2070147Notes

Reaction equation

HRID 2070147 reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[NH:10][C:9](=[O:12])[CH:8]([NH:13]C(=O)C)[CH2:7]2.[ClH:17]>>[ClH:17].[ClH:17].[NH2:13][CH:8]1[CH2:7][C:6]2[C:11](=[C:2]([NH2:1])[CH:3]=[CH:4][CH:5]=2)[NH:10][C:9]1=[O:12]

Participants

3

Conditions

Temperature
110 °C

Procedure

N-(8-Amino-2-oxo-1,2,3,4-tetrahydroquinolin-3-yl)acetamide (8.4 g) was added to concentrated hydrochloric acid (84 mL), and the mixture was heated at 110° C. for three hours while being stirred, followed by stirring under cooling on ice. The formed precipitates were recovered through filtration, and the thus-obtained solid was washed with ethanol, followed by drying, whereby the title compound (9.17 g) was yielded.

Workup

  1. stirringby stirring
  2. temperatureunder cooling on ice
  3. customThe formed precipitates
  4. filtrationwere recovered through filtration
  5. washthe thus-obtained solid was washed with ethanol
  6. customby drying

Sources & evidence

ORD record
ord-65d73bdbd2574308bf8b281452ae0ae2
Source dataset
uspto-grants-2012_10
Patent number
US08299255B2

Reaction notes

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