ChemicalBook--->CAS DataBase List--->1687-51-0

1687-51-0

1687-51-0 Structure

1687-51-0 Structure
IdentificationBack Directory
[Name]

2-Quinazolinamine
[CAS]

1687-51-0
[Synonyms]

2-Quinazolinamine
2-Aminoquinazoline
quinazolin-2-amine
Quinazolin-2-ylamine
Quinazoline, 2-amino-
2-Quinazolinamine (9CI)
[Molecular Formula]

C8H7N3
[MDL Number]

MFCD00956186
[MOL File]

1687-51-0.mol
[Molecular Weight]

145.16
Chemical PropertiesBack Directory
[Melting point ]

204 °C
[Boiling point ]

370.7±25.0 °C(Predicted)
[density ]

1.292±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

solid
[pka]

4.86±0.10(Predicted)
[color ]

Yellow
[NIST Chemistry Reference]

2-Quinazolinamine(1687-51-0)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

2-Quinazolinamine(1687-51-0)MS
2-Quinazolinamine(1687-51-0)1HNMR
2-Quinazolinamine(1687-51-0)IR1
2-Quinazolinamine(1687-51-0)IR2
Hazard InformationBack Directory
[Synthesis]

2-BROMOBENZYLAMINE

3959-05-5

Guanidine hydrochloride

50-01-1

2-Quinazolinamine

1687-51-0

GENERAL STEPS: DMSO (2.0 mL) was added to a 25 mL Schlenk tube protected by nitrogen and equipped with a magnetic stirrer. 2-Bromobenzylamine (1) (0.5 mmol), guanidine hydrochloride (2) (1.0 mmol), CuBr (0.1 mmol, 14.2 mg) and K2CO3 (1.5 mmol, 207 mg) were added sequentially. The reaction mixture was stirred at 80-120 °C for 24 h, followed by continued stirring for 0.5 h in air. After completion of the reaction, the mixture was cooled to room temperature, filtered, and the solid fraction was washed with ethyl acetate (3 x 3 mL). The filtrates were combined and concentrated by rotary evaporator and the residue was purified by silica gel column chromatography using petroleum ether/ethyl acetate as eluent to give the target product 2-aminoquinazoline.

[References]

[1] Synlett, 2013, vol. 24, # 16, p. 2089 - 2094
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