methyl tosylcarbamate
methyl tosylcarbamate Basic information
- Product Name:
- methyl tosylcarbamate
- Synonyms:
-
- methyl tosylcarbamate
- N-(4-Methylphenylsulfonyl)carbamic acid methyl ester
- N-(Methoxycarbonyl)-p-toluenesulfonamide
- N-(p-Tolylsulfonyl)carbamic acid methyl ester
- N-Tosylcarbamic acid methyl ester
- Einecs 238-411-4
- (p-Tolylsulfonyl)carbaMic Acid Methyl Ester
- [(4-Methylphenyl)sulfonyl]carbaMic Acid Methyl Ester
- CAS:
- 14437-03-7
- MF:
- C9H11NO4S
- MW:
- 229.25
- EINECS:
- 238-411-4
- Product Categories:
-
- Aromatics
- Heterocycles
- Impurities
- Sulfur & Selenium Compounds
- Mol File:
- 14437-03-7.mol
methyl tosylcarbamate Chemical Properties
- Melting point:
- 115 °C
- Density
- 1.300±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- DMSO (Slightly), Ethyl Acetate (Slightly) , Methanol (Slightly)
- pka
- 4.76±0.10(Predicted)
- form
- Solid
- color
- White to Off-White
methyl tosylcarbamate Usage And Synthesis
Chemical Properties
Off-White Solid
Uses
N-(p-Tosyl)carbamic Acid Methyl Ester is a degradation product of Gliclazide.
Synthesis
70-55-3
79-22-1
14437-03-7
General method: 4-substituted benzenesulfonamides were dissolved in anhydrous dichloromethane and the solution was cooled to 0°C in an ice bath. Subsequently, trimethylamine was slowly added dropwise to the reaction system. The reaction temperature was maintained at 0 °C and after continuous stirring for 10 min, methyl chloroformate was added dropwise. Stirring of the reaction mixture was continued at 0°C for 30 minutes. The ice bath was removed and the reaction mixture was allowed to gradually warm up to room temperature over 2 hours. Upon completion of the reaction, the reaction mixture was diluted with dichloromethane and the organic phase was washed sequentially with 1 M aqueous hydrochloric acid, water and saturated brine. The organic layer was dried with anhydrous magnesium sulfate and subsequently concentrated under reduced pressure. The residue was purified by silica gel column chromatography to afford the target product, methyl 4-substituted (phenylsulfonyl)carbamate.
References
[1] Journal of the Chinese Chemical Society, 2007, vol. 54, # 3, p. 771 - 777
[2] Organic Process Research and Development, 2016, vol. 20, # 2, p. 440 - 445
[3] Tetrahedron Letters, 2016, vol. 57, # 13, p. 1476 - 1478
[4] Journal of Medicinal Chemistry, 2004, vol. 47, # 3, p. 627 - 643
[5] Journal of Medicinal Chemistry, 2017, vol. 60, # 3, p. 1126 - 1141
methyl tosylcarbamateSupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 400-6009262 16621234537
- chenyj@titansci.com
- Tel
- 021-50135380
- shchemsky@sina.com
- Tel
- 22-58627059 13920586291
- zdcomcon@126.com
- Tel
- 0755-0755-66853366 13670046396
- sales@chem-strong.com
methyl tosylcarbamate(14437-03-7)Related Product Information
- Gliclazide EP Impurity E
- Gliclazide
- Gliclazide Impurity (Methyl N-Methyl-p-Tolysulphoncarbomate)
- Gliclazide EP Impurity G
- N-[[(HEXAHYDROCYCLOPENTA [C]PYRROL-2(1H)-YL)AMINO]CARBONYL]-2-METHYL BENZENESULFONAMIDE
- octahydro-2-nitrosocyclopenta[c]pyrrole
- Gliclazide iMpurity D
- Carboxy Gliclazide
- Ethyl N-(4-methylphenyl)sulfonylcarbamate
- [[4-[2-[[(3-Ethyl-2,5-dihydro-4-methyl-2-oxo-1H-pyrrol-1-yl)carbonyl]amino]ethyl]phenyl]sulfonyl]-carbamic acid ethyl ester
- methyl tosylcarbamate
- N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE
- N-(4-BROMO-2-BUTYNYL)-N-(TERT-BUTYLOXYCARBONYL)(4-METHYLPHENYL)SULFONAMIDE
- 1-(6-METHYL[1,3]THIAZOLO[3,2-B][1,2,4]TRIAZOL-5-YL)ETHYL N-[(4-METHYLPHENYL)SULFONYL]CARBAMATE
- ETHYL 4-[2-(5-CHLORO-2-METHOXYBENZAMIDO)ETHYL]BENZENE SULFONAMIDE CARBAMATE
- 25,27-DIMETHOXY-26-(N-TOSYL)CARBOMOYLOXYCALIX[4]ARENE
- Tosular
- [5-CHLORO-1-METHYL-3-(TRIFLUOROMETHYL)-1H-PYRAZOL-4-YL]METHYL N-[(4-METHYLPHENYL)SULFONYL]CARBAMATE