Basic information Safety Supplier Related

7-Amino-3,4-dihydro-1H-quinolin-2-one

Basic information Safety Supplier Related

7-Amino-3,4-dihydro-1H-quinolin-2-one Basic information

Product Name:
7-Amino-3,4-dihydro-1H-quinolin-2-one
Synonyms:
  • 7-AMINO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE
  • 7-AMINO-3,4-DIHYDRO-2(1H)-QUINOLINONE
  • 7-AMINO-3,4-DIHYDROQUINOLIN-2(1H)-ONE
  • 2(1H)-quinolinone, 7-amino-3,4-dihydro-
  • 7-amino-3,4-dihydroquinolin-2(1H)-one(SALTDATA: FREE)
  • 7-aMino-1,2,3,4-tetrahydroquinolin-2-one
  • 7-AMINO-1,2,3,4-TETRAHYDRO-2-QUINOLINONE
  • 7-Amino-3,4-dihydro-2(1H)
CAS:
22246-07-7
MF:
C9H10N2O
MW:
162.19
Mol File:
22246-07-7.mol
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7-Amino-3,4-dihydro-1H-quinolin-2-one Chemical Properties

Melting point:
213-214 °C
Boiling point:
403.1±45.0 °C(Predicted)
Density 
1.237±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
solid
pka
14.65±0.20(Predicted)
Appearance
Light brown to brown Solid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38-52
Safety Statements 
26
HazardClass 
IRRITANT
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7-Amino-3,4-dihydro-1H-quinolin-2-one Usage And Synthesis

Synthesis

1613720-64-1

22246-07-7

General procedure for the synthesis of 7-amino-3,4-dihydro-2(1H)-quinolinone from the compound (CAS: 1613720-64-1): firstly, a suspension of Pd(OH)2/C (10%, 3.0 g) and ethyl (E)-3-(2,4-dinitrophenyl)acrylate (12.0 g, 45.1 mmol) in MeOH (80 mL) was was stirred at 25°C. The reaction was carried out under H2 (45 psi) atmosphere for 15 hours. Upon completion of the reaction, the mixture was filtered and the filtrate was concentrated under vacuum to afford ethyl 3-(2,4-diaminophenyl)propionate (8.6 g, 98% yield), which was used directly in the next step of the reaction without further purification. Next, a solution of EtOH (50 mL) of ethyl 3-(2,4-diaminophenyl)propanoate (8.6 g, 41.3 mmol) was stirred at 85-100°C for 48 hours. At the end of the reaction, the reaction mixture was cooled to room temperature and the solvent was removed under vacuum. EtOAc (10 mL) was added to the residue and the precipitate was collected by filtration to afford 7-amino-3,4-dihydro-1H-quinolin-2-one (5.8 g, 87% yield). The product was characterized by 1H NMR (DMSO-d6, 400 MHz): δ 9.83 (brs, 1H), 6.76 (d, J = 7.6 Hz, 1H), 6.12 (m, 2H), 4.95 (brs, 2H), 2.65 (t, J = 7.2 Hz, 2H), 2.36 (t, J = 7.2 Hz, 2H).

References

[1] Patent: US2014/206663, 2014, A1. Location in patent: Paragraph 1265; 1266

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