ChemicalBook--->CAS DataBase List--->5577-13-9

5577-13-9

5577-13-9 Structure

5577-13-9 Structure
IdentificationBack Directory
[Name]

Ethyl N-(4-methylphenyl)sulfonylcarbamate
[CAS]

5577-13-9
[Synonyms]

Tosylurethane
ethyl tosylcarbaMate
Gliclazide IMpurity C
Gliclazide EP Impurity C
Tosylcarbamic acid ethyl ester
Ethyl [(4-Methylphenyl)sulphonyl]ca
ethyl n-(4-methylphenyl)sulfonylcarbamate
Ethyl [(4-methylphenyl)sulphonyl]carbamate
Ethyl [(4-methylphenyl)sulfonyl]-carbamate
N-(p-Tolylsulfonyl)carbamic acid ethyl ester
Gliclazide Impurity 3(Gliclazide EP Impurity C)
N-(4-methylphenyl)sulfonylcarbamic acid ethyl ester
3-ethyl-4-methylbenzenesulfonic acid carbamoyl ester
Carbamic acid, N-[(4-methylphenyl)sulfonyl]-, ethyl ester
[EINECS(EC#)]

226-952-9
[Molecular Formula]

C10H13NO4S
[MDL Number]

MFCD00797861
[MOL File]

5577-13-9.mol
[Molecular Weight]

243.28
Chemical PropertiesBack Directory
[Melting point ]

82-84oC
[Boiling point ]

272℃ at 100.8-101kPa
[density ]

1.38 at 20℃
[vapor pressure ]

1.8-7.9Pa at 20-25℃
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly), Ethyl Acetate (Slightly)
[form ]

Solid
[color ]

White
[LogP]

0.73-1.7 at 23℃ and pH2-7
[Surface tension]

63.8mN/m at 1g/L and 20℃
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
[REACH Registrations]

Active
Hazard InformationBack Directory
[Uses]

Tosylurethane (Gliclazide EP Impurity C) is an intermediate in the synthesis of Gliclazide (G409877), a sulfonylurea hypoglycemic agent. Used as an antidiabetic.
[Synthesis]

Ethanol

64-17-5

Carbamic acid, N-[(4-methylphenyl)sulfonyl]-, butyl ester

31224-37-0

Ethyl N-(4-methylphenyl)sulfonylcarbamate

5577-13-9

GENERAL STEPS: Dissolve 4-methylphenylsulfonylcarbamate (Compound, CAS:31224-37-0) in selected alcohol (ethanol, 2 mL) in a microwaveable reaction vial. The reaction vial was sealed using an aluminum cap with a PTFE-faced septum. The reaction mixture was placed in a microwave reactor and radiantly heated at 100-120°C for 20-60 min. Upon completion of the reaction, the crude product was concentrated under reduced pressure and the residue was subsequently purified by silica gel column chromatography to finally obtain the target product, ethyl N-(4-methylphenyl)sulfonylcarbamate.

[References]

[1] Tetrahedron Letters, 2016, vol. 57, # 13, p. 1476 - 1478
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