Methyl 3-benzenesulfonaMidobenzoate

Methyl 3-benzenesulfonaMidobenzoate Suppliers list
Company Name: Adamas Reagent, Ltd.  
Tel: 400-6009262 15618770481
Email: yhx@titansci.com
Company Name: Hunan Hui Bai Shi Biotechnology Co., Ltd.  
Tel: 0731-85526065 13308475853
Email: ivy@hnhbsj.com
Company Name: Chengdu HappySyn Pharmaceutical Technology Co., Ltd.  
Tel: 85114309 18982182443
Email: yangli@happysyn.com
Company Name: 9ding chemical ( Shanghai) Limited  
Tel: 4009209199
Email: sales@9dingchem.com
Company Name: Zhengzhou Guancheng Laboratory equipment Sales  
Tel: 0371-88888888 qq272369594;2159423853qq
Email: 2723695949@qq.com
Methyl 3-benzenesulfonaMidobenzoate Basic information
Product Name:Methyl 3-benzenesulfonaMidobenzoate
Synonyms:Methyl 3-benzenesulfonaMidobenzoate;methyl 3-(phenylsulfonamido)benzoate;Benzoic acid, 3-[(phenylsulfonyl)amino]-, methyl ester;3-(phenylsulfonylacylamino)methyl benzoate
CAS:107922-46-3
MF:C14H13NO4S
MW:291.32
EINECS:
Product Categories:
Mol File:107922-46-3.mol
Methyl 3-benzenesulfonaMidobenzoate Structure
Methyl 3-benzenesulfonaMidobenzoate Chemical Properties
Boiling point 448.1±47.0 °C(Predicted)
density 1.345±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka7.79±0.10(Predicted)
Safety Information
MSDS Information
Methyl 3-benzenesulfonaMidobenzoate Usage And Synthesis
Synthesis
METHYL 3-AMINOBENZOATE

4518-10-9

Benzenesulfonyl chloride

98-09-9

Methyl 3-benzenesulfonaMidobenzoate

107922-46-3

Methyl 3-aminobenzoate (10 g, 66.2 mmol) was dissolved in pyridine (100 mL) and cooled in an ice bath for 15 minutes. Benzenesulfonyl chloride (8.53 mL, 66.2 mmol) was added slowly dropwise over 5 min using a syringe, followed by stirring the reaction mixture and gradually warming it to room temperature, the reaction lasted for 16 hours. The reaction mixture was slowly poured into a 1 M HCl solution (250 mL total volume) containing ice and the pH was adjusted to 2-3 to form a heterogeneous acidic mixture. The precipitate was collected by filtration and washed with plenty of water. The resulting solid was dried under high vacuum for 12 h to give the target product methyl 3-benzenesulfonylaminobenzoate (19.3 g, 100% yield) as an off-white solid.

References[1] Patent: WO2010/126922, 2010, A1. Location in patent: Page/Page column 26
[2] Journal of Medicinal Chemistry, 2009, vol. 52, # 10, p. 3317 - 3327
[3] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 15, p. 4436 - 4440
Methyl 3-benzenesulfonaMidobenzoate Preparation Products And Raw materials
Raw materialsPhenylboronic acid-->Methyl 3-aminobenzoate-->Benzenesulfonyl chloride-->Methyl 3-nitrobenzoate
Tag:Methyl 3-benzenesulfonaMidobenzoate(107922-46-3) Related Product Information
3-(((4-Methylphenyl)sulfonyl)amino)benzoic acid 3-Benzenesulfonylaminobenzoic acid N-(3-Formylphenyl)benzenesulfonamide Methyl 4-(phenylsulfonaMido)benzoate Benzoic acid, 4-[[(4-methylphenyl)sulfonyl]amino]-, methyl ester 3-(4-Bromo-benzenesulfonylamino)-benzoic acid