ChemicalBook > Product Catalog >Analytical Chemistry >Standard >Pharmaceutical Impurity Reference Standards >1-Azetidinesulfonamide(9CI)

1-Azetidinesulfonamide(9CI)

1-Azetidinesulfonamide(9CI) Suppliers list
Company Name: Wuxi Donghe Pharmaceutical Technology Co., Ltd.  Gold
Tel: 63313187 15358055255
Email: 63313187@qq.com
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  Gold
Tel: 18149758185 18149758185
Email: sales-cpd@caerulumpharma.com
Company Name: shanghaiaoderuikanglimitedcompany  Gold
Tel: 18902198068 18912886236
Email: akslichenglong@163.com
Company Name: skychemical Co.Ltd  
Tel: 021-20958197 20965099
Email: sales@skychemical.com
Company Name: ChemShuttle, Inc.  
Tel: 0510-83588313-811 18800520310
Email: sales@chemshuttle.com
1-Azetidinesulfonamide(9CI) Basic information
Product Name:1-Azetidinesulfonamide(9CI)
Synonyms:azetidine-1-sulfonaMide;1-Azetidinesulfonamide;1-Azetidinesulfonamide(9CI);102882;azetidine-1-sulphonamide;CPD1543-A9;azetidine-1-sulfonamide - [A87170]
CAS:654073-32-2
MF:C3H8N2O2S
MW:136.17
EINECS:
Product Categories:SULFONAMIDE
Mol File:654073-32-2.mol
1-Azetidinesulfonamide(9CI) Structure
1-Azetidinesulfonamide(9CI) Chemical Properties
Boiling point 276.3±23.0 °C(Predicted)
density 1.51±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
pka11.52±0.20(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C3H8N2O2S/c4-8(6,7)5-2-1-3-5/h1-3H2,(H2,4,6,7)
InChIKeySTIUWSWFXIBBKI-UHFFFAOYSA-N
SMILESN1(S(N)(=O)=O)CCC1
Safety Information
MSDS Information
1-Azetidinesulfonamide(9CI) Usage And Synthesis
Synthesis
benzyl(azetidin-1-ylsulfonyl)carbamate

1271835-78-9

1-Azetidinesulfonamide(9CI)

654073-32-2

The general procedure for the synthesis of 1-azetidinylsulfonamide using the compound (CAS:1271835-78-9) as starting material was as follows: palladium hydroxide (20%, 350 mg), benzyl (azetidin-1-ylsulfonyl) carbamate (1.49 g, 5.5 mmol), and 1-methyl-1,4-cyclohexadiene (10.7 g, 0.11 mol) of the The mixture was dissolved in methanol (35 mL) and the reaction was stirred at 60 °C under nitrogen protection overnight. After completion of the reaction, the mixture was cooled to room temperature, filtered through a diatomaceous earth pad, and the filtrate was concentrated in vacuum to afford 1-azetidinesulfonamide (437 mg, 58% yield) as a solid product. The product was characterized by 1H NMR (400 MHz, CD3OD) with chemical shifts δ of 2.15 (quintuple peak, 2H) and 3.78 (triplet peak, 4H).The corresponding mass ions were not detected by LCMS analysis.

References[1] Patent: WO2013/88315, 2013, A1. Location in patent: Page/Page column 75
[2] Patent: WO2013/102826, 2013, A1. Location in patent: Page/Page column 91
1-Azetidinesulfonamide(9CI) Preparation Products And Raw materials
Raw materialsbenzyl(azetidin-1-ylsulfonyl)carbamate-->Palladium hydroxide-->1-Methyl-1,4-cyclohexadiene-->Methanol
Tag:1-Azetidinesulfonamide(9CI)(654073-32-2) Related Product Information
3-methylazetidine-1-sulfonamide 1-Azetidinesulfonamide, 3-amino- 1-Azetidinesulfonamide, 3-(aminomethyl)- 3-fluoroazetidine-1-sulfonaMide 1-Azetidinesulfonamide, 3-oxo- 1-Azetidinesulfonamide, 3-hydroxy-