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6-Chloroquinazoline-2,4(1H,3H)-dione

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6-Chloroquinazoline-2,4(1H,3H)-dione Basic information

Product Name:
6-Chloroquinazoline-2,4(1H,3H)-dione
Synonyms:
  • 6-Chloroquinazoline-2,4(1H,3H)-dione
  • 6-Chloroquinazoline-2,4-dione
  • 6-chloroquinazoline-2,4-diol
  • 6-chloro-1,2,3,4-tetrahydroquinazoline-2,4-dione
  • 6-Chloro-2,4-dioxo-1,2,3,4-tetrahydroquinazoline
  • 6-Chloro-2,4-quinazolinediol
  • 6-Chloroquinazolin-2,4(1H,3H)-dione
  • NSC 194820
CAS:
1640-60-4
MF:
C8H5ClN2O2
MW:
196.59
Product Categories:
  • blocks
  • Quinolines
Mol File:
1640-60-4.mol
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6-Chloroquinazoline-2,4(1H,3H)-dione Chemical Properties

Melting point:
360℃ (acetic acid )
Density 
1.475±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
10.02±0.20(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C8H5ClN2O2/c9-4-1-2-6-5(3-4)7(12)11-8(13)10-6/h1-3H,(H2,10,11,12,13)
InChIKey
IGWJEWGQUFOVDP-UHFFFAOYSA-N
SMILES
N1C2=C(C=C(Cl)C=C2)C(=O)NC1=O
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Safety Information

Hazard Codes 
Xi
HS Code 
2933599590
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6-Chloroquinazoline-2,4(1H,3H)-dione Usage And Synthesis

Synthesis

124-38-9

5922-60-1

1640-60-4

Under argon protection, 2-amino-5-chlorobenzonitrile (1 mmol) was dissolved in DMSO-d6 (1 mL), catalyst (0.01 mmol) was added and placed in a stainless steel autoclave. The autoclave was sealed, heated to 110 °C, and then carbon dioxide was introduced to reach a pressure of 2 MPa. The reaction mixture was subjected to cyclization by magnetic stirring at 110 °C for 3 h. After the reaction was completed, the autoclave was placed in the autoclave and the catalyst was added to the reaction mixture. Upon completion of the reaction, the autoclave was cooled in an ice bath and the pressure was slowly released. The chemical yield of 6-chloroquinazoline-2,4-dione was determined by 1H NMR analysis using 3,5-dimethoxybenzyl alcohol as an internal standard. Following the same procedure, a DMSO solution (6 mL) of 2-amino-5-chlorobenzonitrile (6 mmol) was subjected to a carboxycyclization reaction with carbon dioxide. After the reaction, the autoclave was cooled and depressurized and the reaction mixture was poured into water (60 mL). The precipitate was collected by filtration, washed sequentially with water and ether, and finally dried under vacuum at 35 °C for 15 h to give pure 6-chloroquinazoline-2,4-dione.

References

[1] Heteroatom Chemistry, 2012, vol. 23, # 3, p. 276 - 280
[2] RSC Advances, 2015, vol. 5, # 7, p. 5032 - 5037
[3] Tetrahedron, 2018, vol. 74, # 24, p. 2914 - 2920
[4] Green Chemistry, 2014, vol. 16, # 6, p. 3142 - 3148
[5] Tetrahedron, 2002, vol. 58, # 16, p. 3155 - 3158

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