Product Name

  • Name

    Gliquidone

  • EINECS 251-463-2
  • CAS No. 33342-05-1
  • Article Data73
  • CAS DataBase
  • Density 1.34 g/cm3
  • Solubility
  • Melting Point 179 °C
  • Formula C27H33N3O6S
  • Boiling Point
  • Molecular Weight 527.642
  • Flash Point
  • Transport Information
  • Appearance white powder
  • Safety 24/25
  • Risk Codes
  • Molecular Structure Molecular Structure of 33342-05-1 (Gliquidone)
  • Hazard Symbols
  • Synonyms AR-DF 26;ARDF 26SE;Beglynor;Glurenorm;
  • PSA 130.26000
  • LogP 5.31900

Synthetic route

4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonamid
33456-68-7

4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonamid

Cyclohexyl isocyanate
3173-53-3

Cyclohexyl isocyanate

gliquidone
33342-05-1

gliquidone

Conditions
ConditionsYield
Stage #1: 4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonamid With potassium carbonate at 40℃; for 0.5h;
Stage #2: Cyclohexyl isocyanate at 90℃; for 4.5h; Reagent/catalyst; Temperature;
80%
gliquidone
33342-05-1

gliquidone

N-Cyclohexyl-N',N''-bis-<4-<2-(3,4-dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonyl>guanidin

N-Cyclohexyl-N',N''-bis-<4-<2-(3,4-dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonyl>guanidin

Conditions
ConditionsYield
With pyridine; p-toluenesulfonyl chloride Heating;81%
gliquidone
33342-05-1

gliquidone

4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonamid
33456-68-7

4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonamid

Conditions
ConditionsYield
With dmap; phthalic anhydride In pyridine for 5h; Reflux; Inert atmosphere;77%
With pyridine; dmap; phthalic anhydride for 5h; Inert atmosphere; Reflux;77%
With pyridine; dmap; phthalic anhydride for 4h; Inert atmosphere; Reflux;75%
gliquidone
33342-05-1

gliquidone

acetic anhydride
108-24-7

acetic anhydride

N-<4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonyl>acetamid

N-<4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonyl>acetamid

Conditions
ConditionsYield
With pyridine for 0.25h;71%
phthalic anhydride
85-44-9

phthalic anhydride

gliquidone
33342-05-1

gliquidone

A

4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonamid
33456-68-7

4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonamid

B

N-cyclohexylphthalimide
2133-65-5

N-cyclohexylphthalimide

Conditions
ConditionsYield
With pyridine; dmap for 4h; Heating;A 46%
B 46%
gliquidone
33342-05-1

gliquidone

A

4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonamid
33456-68-7

4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonamid

B

N-cyclohexylphthalimide
2133-65-5

N-cyclohexylphthalimide

Conditions
ConditionsYield
With pyridine; dmap; phthalic anhydride for 4h; Heating;A 46%
B 46%
succinic acid anhydride
108-30-5

succinic acid anhydride

gliquidone
33342-05-1

gliquidone

N-<4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonyl>succinimid

N-<4-<2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl>benzolsulfonyl>succinimid

Conditions
ConditionsYield
With pyridine; dmap32%
gliquidone
33342-05-1

gliquidone

nickel(II) chloride hexahydrate

nickel(II) chloride hexahydrate

Ni(gliquidone)2Cl2

Ni(gliquidone)2Cl2

Conditions
ConditionsYield
In methanol MeOH soln. of metal salt added to gliquidone soln. with stirring, warmedto ca. 60°C; filtered, washed, dried; elem. anal.;
copper(II) choride dihydrate

copper(II) choride dihydrate

gliquidone
33342-05-1

gliquidone

Cu(gliquidone)2Cl2

Cu(gliquidone)2Cl2

Conditions
ConditionsYield
In methanol MeOH soln. of metal salt added to gliquidone soln. with stirring, warmedto ca. 60°C; filtered, washed, dried; elem. anal.;
iron(III) chloride hexahydrate

iron(III) chloride hexahydrate

gliquidone
33342-05-1

gliquidone

Fe(gliquidone)2Cl3

Fe(gliquidone)2Cl3

Conditions
ConditionsYield
In methanol MeOH soln. of metal salt added to gliquidone soln. with stirring, warmedto ca. 60°C; filtered, washed, dried; elem. anal.;
gliquidone
33342-05-1

gliquidone

chromium chloride hexahydrate

chromium chloride hexahydrate

Cr(gliquidone)2Cl2

Cr(gliquidone)2Cl2

Conditions
ConditionsYield
In methanol MeOH soln. of metal salt added to gliquidone soln. with stirring, warmedto ca. 60°C; filtered, washed, dried; elem. anal.;
gliquidone
33342-05-1

gliquidone

cadmium(II) chloride monohydrate

cadmium(II) chloride monohydrate

Cd(gliquidone)2Cl2

Cd(gliquidone)2Cl2

Conditions
ConditionsYield
In methanol MeOH soln. of metal salt added to gliquidone soln. with stirring, warmedto ca. 60°C; filtered, washed, dried; elem. anal.;
gliquidone
33342-05-1

gliquidone

manganese(II) chloride monohydrate

manganese(II) chloride monohydrate

Mn(gliquidone)2Cl2

Mn(gliquidone)2Cl2

Conditions
ConditionsYield
In methanol MeOH soln. of metal salt added to gliquidone soln. with stirring, warmedto ca. 60°C; filtered, washed, dried; elem. anal.;
gliquidone
33342-05-1

gliquidone

cobalt(II) chloride hexahydrate

cobalt(II) chloride hexahydrate

Co(gliquidone)2Cl2

Co(gliquidone)2Cl2

Conditions
ConditionsYield
In methanol MeOH soln. of metal salt added to gliquidone soln. with stirring, warmedto ca. 60°C; filtered, washed, dried; elem. anal.;
gliquidone
33342-05-1

gliquidone

zinc(II) chloride
7646-85-7

zinc(II) chloride

Zn(gliquidone)2Cl2

Zn(gliquidone)2Cl2

Conditions
ConditionsYield
In methanol MeOH soln. of metal salt added to gliquidone soln. with stirring, warmedto ca. 60°C; filtered, washed, dried; elem. anal.;
gliquidone
33342-05-1

gliquidone

C22H22N6O5S2*C27H33N3O6S

C22H22N6O5S2*C27H33N3O6S

Conditions
ConditionsYield
In methanol Reflux;
piperazine
110-85-0

piperazine

gliquidone
33342-05-1

gliquidone

2-methyl-propan-1-ol
78-83-1

2-methyl-propan-1-ol

2C27H33N3O6S*C4H10N2*2C4H10O

2C27H33N3O6S*C4H10N2*2C4H10O

Conditions
ConditionsYield
at 20 - 50℃; for 13h;
piperazine
110-85-0

piperazine

gliquidone
33342-05-1

gliquidone

ethanol
64-17-5

ethanol

2C27H33N3O6S*C4H10N2*2C2H6O

2C27H33N3O6S*C4H10N2*2C2H6O

Conditions
ConditionsYield
at 20 - 50℃; for 13h;
piperazine
110-85-0

piperazine

gliquidone
33342-05-1

gliquidone

acetonitrile
75-05-8

acetonitrile

2C27H33N3O6S*C4H10N2*C2H3N

2C27H33N3O6S*C4H10N2*C2H3N

Conditions
ConditionsYield
at 20 - 50℃; for 13h;
piperazine
110-85-0

piperazine

gliquidone
33342-05-1

gliquidone

isopropyl alcohol
67-63-0

isopropyl alcohol

2C27H33N3O6S*C4H10N2*2C3H8O

2C27H33N3O6S*C4H10N2*2C3H8O

Conditions
ConditionsYield
at 20 - 50℃; for 13h;
piperazine
110-85-0

piperazine

methanol
67-56-1

methanol

gliquidone
33342-05-1

gliquidone

2C27H33N3O6S*C4H10N2*2CH4O

2C27H33N3O6S*C4H10N2*2CH4O

Conditions
ConditionsYield
at 20 - 50℃; for 13h;
gliquidone
33342-05-1

gliquidone

dimethylbiguanide
657-24-9

dimethylbiguanide

C4H12N5(1+)*C27H32N3O6S(1-)

C4H12N5(1+)*C27H32N3O6S(1-)

Conditions
ConditionsYield
In acetonitrile at 20℃; for 24h; Solvent; Temperature; Sonication;

Gliquidone Specification

The Gliquidone, with the CAS registry number 33342-05-1 and EINECS registry number 251-463-2, has the IUPAC name of 1-cyclohexyl-3-[4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxoisoquinolin-2-yl)ethyl]phenyl]sulfonylurea. It belongs to the product categories of Active Pharmaceutical Ingredients and API. And the molecular formula of the chemical is C27H33N3O6S. What's more, it is an anti-diabetic drug in the sulfonylurea class, and always used in the treatment of diabetes mellitus type 2.

The physical properties of Gliquidone are as followings: (1)ACD/LogP: 3.11; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): 1.94; (4)ACD/LogD (pH 7.4): 1.14; (5)ACD/BCF (pH 5.5): 9.23; (6)ACD/BCF (pH 7.4): 1.47; (7)ACD/KOC (pH 5.5): 79.48; (8)ACD/KOC (pH 7.4): 12.62; (9)#H bond acceptors: 9; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 6; (12)Polar Surface Area: 112.68 Å2; (13)Index of Refraction: 1.624; (14)Molar Refractivity: 138.9 cm3; (15)Molar Volume: 393.2 cm3; (16)Polarizability: 55.06×10-24cm3; (17)Surface Tension: 62.7 dyne/cm; (18)Density: 1.34 g/cm3.

Uses of Gliquidone: It can react with acetic acid anhydride to produce N-{4-[2-(3,4-Dihydro-7-methoxy-4,4-dimethyl-1,3-dioxo-2(1H)-isochinolyl)ethyl]benzolsulfonyl}acetamid. This reaction will need reagent pyridine. The reaction time is 15 minutes, and the yield is about 71%.    

You can still convert the following datas into molecular structure:
(1)SMILES: O=C(NC1CCCCC1)NS(=O)(=O)c2ccc(cc2)CCN4C(=O)c3c(ccc(OC)c3)C(C4=O)(C)C
(2)InChI: InChI=1/C27H33N3O6S/c1-27(2)23-14-11-20(36-3)17-22(23)24(31)30(25(27)32)16-15-18-9-12-21(13-10-18)37(34,35)29-26(33)28-19-7-5-4-6-8-19/h9-14,17,19H,4-8,15-16H2,1-3H3,(H2,28,29,33)
(3)InChIKey: LLJFMFZYVVLQKT-UHFFFAOYAT

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