Product Name

  • Name

    Satranidazole

  • EINECS
  • CAS No. 56302-13-7
  • Article Data3
  • CAS DataBase
  • Density 1.77g/cm3
  • Solubility
  • Melting Point 185°C
  • Formula C8H11 N5 O5 S
  • Boiling Point 505.2°Cat760mmHg
  • Molecular Weight 289.272
  • Flash Point 259.3°C
  • Transport Information
  • Appearance
  • Safety Slightly toxic by ingestion. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx and SOx.
  • Risk Codes
  • Molecular Structure Molecular Structure of 56302-13-7 (Satranidazole)
  • Hazard Symbols
  • Synonyms CG 10213Go;Go 10213; Satranidazole
  • PSA 129.71000
  • LogP 1.13680

Synthetic route

1-(methylsulphonyl)-2-oxo-2,3,4,5-tetrahydroimidazole
41730-79-4

1-(methylsulphonyl)-2-oxo-2,3,4,5-tetrahydroimidazole

1-methyl-2-methylsulphonyl-5-nitro-imidazole
1615-53-8

1-methyl-2-methylsulphonyl-5-nitro-imidazole

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one
56302-13-7

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide at 25℃; for 5h;80%
1-methylsulphonyl-3-(1-methyl-2-imidazolyl)-2-imidazolidinone
85695-00-7

1-methylsulphonyl-3-(1-methyl-2-imidazolyl)-2-imidazolidinone

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one
56302-13-7

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one

Conditions
ConditionsYield
With sulfuric acid; nitric acid at 120℃; for 1.5h;15 mg
2-chloro-1-methyl-5-nitroimidazole
86072-07-3

2-chloro-1-methyl-5-nitroimidazole

1-(methylsulphonyl)-2-oxo-2,3,4,5-tetrahydroimidazole
41730-79-4

1-(methylsulphonyl)-2-oxo-2,3,4,5-tetrahydroimidazole

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one
56302-13-7

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide 1.) 30 min, room temperature, 2.) a) 1 h, room temperture, b) 3 h, 55 deg C, c) room temperature;0.9 g
1-(1-methyl-imidazolyl)-2-imidazolidinone hydrochloride

1-(1-methyl-imidazolyl)-2-imidazolidinone hydrochloride

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one
56302-13-7

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 0.1 g / NaH / dimethylformamide; dioxane / 1) 0-5 deg C, 1 h, 2) RT, 12 h
2: 15 mg / conc. H2SO4, HNO3 (d 1.42) / 1.5 h / 120 °C
View Scheme
triethyloxonium fluoroborate
368-39-8

triethyloxonium fluoroborate

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one
56302-13-7

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one

3-ethyl-1-methyl-5-nitro-2-(3-methylsulphonyl-2-oxotetrahydroimidazolyl-1-) imidazolium fluoroborate

3-ethyl-1-methyl-5-nitro-2-(3-methylsulphonyl-2-oxotetrahydroimidazolyl-1-) imidazolium fluoroborate

Conditions
ConditionsYield
In chloroform for 72h; Ambient temperature;0.85 g
1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one
56302-13-7

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one

5'-Amino-3-methanesulfonyl-1'-methyl-4,5-dihydro-3H,1'H-[1,2']biimidazolyl-2-one

5'-Amino-3-methanesulfonyl-1'-methyl-4,5-dihydro-3H,1'H-[1,2']biimidazolyl-2-one

Conditions
ConditionsYield
With hydrogen; sodium sulfate; nickel In ethyl acetate; N,N-dimethyl-formamide at 45℃;
With hydrogenchloride; zinc
1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one
56302-13-7

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one

2-(2-methanesulphonamidoethylamino)-1-methyl-5-nitroimidazole
134307-48-5

2-(2-methanesulphonamidoethylamino)-1-methyl-5-nitroimidazole

Conditions
ConditionsYield
With hydroxide0.1 g
1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one
56302-13-7

1 (1 methyl 5 nitroimidazol 2 yl) 3 (methylsulfonyl)imidazolidin 2 one

A

1-methanesulphonyl-3-(5-nitro-1H-imidazol-2-yl)-2-imidazolidinone
85695-08-5

1-methanesulphonyl-3-(5-nitro-1H-imidazol-2-yl)-2-imidazolidinone

B

1-methanesulphonyl-3-(1-methyl-4-nitro-1H-imidazol-2-yl)-2-imidazolidinone
56302-24-0

1-methanesulphonyl-3-(1-methyl-4-nitro-1H-imidazol-2-yl)-2-imidazolidinone

Conditions
ConditionsYield
With potassium iodide In N,N-dimethyl-formamide for 20h; Heating;A 1.8 g
B 2.1 g
With potassium iodide In N,N-dimethyl-formamide Heating;

SATRANIDAZOLE Chemical Properties

Synonyms: 1-(1-Methyl-5-nitro-1H-imidazol-2-yl)-3-(methylsulfonyl)-2-imidazolidinone;CG-10213Go;Go-10213 Satranidazole;
The Molecular formula of SATRANIDAZOLE(56302-13-7): C8H11N5O5S
Molecular Structure : 
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