ChemicalBook--->CAS DataBase List--->22246-07-7

22246-07-7

22246-07-7 Structure

22246-07-7 Structure
IdentificationBack Directory
[Name]

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

22246-07-7
[Synonyms]

7-Amino-3,4-dihydro-2(1H)
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
Benzenamine,7-hydrazinyl-N,N-dimethyl-
2(1H)-quinolinone, 7-amino-3,4-dihydro-
7-aMino-1,2,3,4-tetrahydroquinolin-2-one
7-AMINO-1,2,3,4-TETRAHYDRO-2-QUINOLINONE
7-amino-3,4-dihydroquinolin-2(1H)-one(SALTDATA: FREE)
[Molecular Formula]

C9H10N2O
[MDL Number]

MFCD06809628
[MOL File]

22246-07-7.mol
[Molecular Weight]

162.19
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37/38-52
[Safety Statements ]

26
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

7-Amino-3,4-dihydro-1H-quinolin-2-one(22246-07-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Benzenepropanoic acid, 2,4-diamino-, ethyl ester

1613720-64-1

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

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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