4-(Methylsulfonylamino)benzylaminehydrochloride

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4-(Methylsulfonylamino)benzylaminehydrochloride Basic information
Product Name:4-(Methylsulfonylamino)benzylaminehydrochloride
Synonyms:N-[4-(Aminomethyl)phenyl]methanesulphonamide hydrochloride;N-[4-(Aminomethyl)phenyl]methanesulphonamide hydrochloride 95+%;N-(4-(AMinoMethyl)phenyl)MethanesulfonaMide hydrochloride;4-[(Methylsulphonyl)amino]benzylamine hydrochloride, 4-(Methylsulphonamido)benzylamine hydrochloride;4-(Methylsulfonylamino)benzylamine, HCl;4-(Methylsulfonylamino)benzylamine hydrochloride(Methylsulfonylamino)Benzylaminehydrochloride;Methanesulfonamide, N-[4-(aminomethyl)phenyl]-, hydrochloride (1:1)
CAS:128263-66-1
MF:C8H13ClN2O2S
MW:236.72
EINECS:
Product Categories:
Mol File:128263-66-1.mol
4-(Methylsulfonylamino)benzylaminehydrochloride Structure
4-(Methylsulfonylamino)benzylaminehydrochloride Chemical Properties
Melting point >275℃ (dec.)
storage temp. Inert atmosphere,Room Temperature
form solid
color White
Safety Information
HazardClass IRRITANT
HS Code 2935909099
MSDS Information
4-(Methylsulfonylamino)benzylaminehydrochloride Usage And Synthesis
Synthesis
Carbamic acid, N-[[4-[(methylsulfonyl)amino]phenyl]methyl]-, 1,1-dimethylethyl ester

238427-63-9

4-(METHYLSULFONYLAMINO)BENZYLAMINEHYDROCHLORIDE

128263-66-1

Step 4: Synthesis of 4-methanesulfonylaminobenzylcarbamate hydrochloride; To a 50 mL single-necked round-bottomed flask was added tert-butyl 4-methanesulfonylaminobenzylcarbamate (1.2 g, 4.0 mmol) and 30 mL of 1,4-dioxane. Concentrated hydrochloric acid (2 mL) was slowly added to the solution and the reaction was stirred for 4 hours at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the reaction mixture was concentrated under reduced pressure to remove the solvent. The resulting solid was washed with ethyl acetate and separated by filtration through a glass filter. Finally, the collected solid was dried in air to afford the target product 4-methylsulfonylaminobenzylamine hydrochloride (0.947 g, 100% yield).

References[1] Patent: WO2006/98554, 2006, A1. Location in patent: Page/Page column 44
4-(Methylsulfonylamino)benzylaminehydrochloride Preparation Products And Raw materials
Raw materialsCarbamic acid, N-[[4-[(methylsulfonyl)amino]phenyl]methyl]-, 1,1-dimethylethyl ester-->Hydrochloric acid-->1,4-Dioxane-->Water
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