2-AMINO-N-METHYLBENZENESULFONAMIDE

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Products Intro: CAS:16288-77-0
Purity:98% Package:g-Kg Remarks:Light brown solid
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Products Intro: Product Name:2-Amino-N-methylbenzenesulfonamide
CAS:16288-77-0
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CAS:16288-77-0
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Products Intro: Product Name:N-Methyl 2-aminobenzenesulfonamide
CAS:16288-77-0
Purity:98% Package:$53.9/250mg;$176.9/1g;$795.9/5g;$3580.9/25g;Bulk package Remarks:98%

2-AMINO-N-METHYLBENZENESULFONAMIDE manufacturers

2-AMINO-N-METHYLBENZENESULFONAMIDE Basic information
Product Name:2-AMINO-N-METHYLBENZENESULFONAMIDE
Synonyms:2-amino-N-methylbenzenesulfonamide(SALTDATA: HCl);N-Methyl-2-aminobenzenesulfonamide;2-aMino-N-Methylbenzene-1-sulfonaMide;BenzenesulfonaMide, 2-aMino-N-Methyl-;2-AMINO-N-METHYLBENZENESULFONAMIDE
CAS:16288-77-0
MF:C7H10N2O2S
MW:186.23
EINECS:
Product Categories:
Mol File:16288-77-0.mol
2-AMINO-N-METHYLBENZENESULFONAMIDE Structure
2-AMINO-N-METHYLBENZENESULFONAMIDE Chemical Properties
Melting point 59-60℃
Boiling point 352.9±44.0 °C(Predicted)
density 1.308
storage temp. 2-8°C(protect from light)
pka11?+-.0.10(Predicted)
AppearanceLight yellow to brown Solid
Safety Information
MSDS Information
2-AMINO-N-METHYLBENZENESULFONAMIDE Usage And Synthesis
Description2-Amino-N-methylbenzenesulfonamide is obtained by treating 2-nitrobenzenesulfonyl chloride with methylamine and subsequent reduction. Used as a dye component. The amides of 2-aminobenzenesulfonic acid can be treated with aldehydes or orthoformic acid esters to give 1,2,4-benzothiadiazine 1,1-dioxides or their dihydro compounds; these substances have been proposed as diuretics.
Synthesis
N-Methyl-2-nitrobenzenesulphonamide

23530-40-7

2-AMINO-N-METHYLBENZENESULFONAMIDE

16288-77-0

Step B / Intermediate C4: Synthesis of 2-amino-N-methylbenzenesulfonamide To a solution of N-methyl-2-nitrobenzenesulfonamide (26 g, 0.12 mol) in methanol (500 mL) was added 10% palladium carbon catalyst (2 g). The reaction mixture was stirred at room temperature under hydrogen atmosphere for 3 hours. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to afford the target product 2-amino-N-methylbenzenesulfonamide (22 g, 98% yield). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 7.45-7.48 (dd, 1H, J=1.6 Hz, 8.0 Hz), 7.24-7.31 (m, 2H), 6.81-6.83 (dd, 1H, J=0.6 Hz, 8.0 Hz), 6.60-6.65 (m, 1H), 5.89 (s 2H), 2.370-2.374 (d, 3H, J=1.6Hz).

References[1] Patent: WO2012/92880, 2012, A1. Location in patent: Page/Page column 64
[2] Angewandte Chemie - International Edition, 2010, vol. 49, # 29, p. 4955 - 4957
[3] Patent: WO2007/45868, 2007, A1. Location in patent: Page/Page column 47
[4] Farmaco, Edizione Scientifica, 1954, vol. 9, p. 661,678, 680
[5] Farmaco, Edizione Scientifica, 1957, vol. 12, p. 495,499, 500
2-AMINO-N-METHYLBENZENESULFONAMIDE Preparation Products And Raw materials
Raw materialsN-Methyl-2-nitrobenzenesulphonamide-->Hydrogen-->Methanol
Preparation ProductsBenzenesulfonaMide, 2-[(2,5-dichloro-4-pyriMidinyl)aMino]-N-Methyl-
Tag:2-AMINO-N-METHYLBENZENESULFONAMIDE(16288-77-0) Related Product Information
Chlorothiazide CYCLOTHIAZIDE DIAZOXIDE Althiazide HYDROFLUMETHIAZIDE Hydrochlorothiazide 2-Amino-N-ethylbenzenesulfonanilide POLYTHIAZIDE (200 MG) Trichlormethiazide BENDROFLUMETHIAZIDE BENZTHIAZIDE 7-(DIMETHYLAMINOSULPHONYL)-2,3-DIHYDRO-1-[[N-(2-METHOXYPHENYL)AMINO]CARBONYL]-(1H)-INDOLE (2-INDOL-3-YLETHYL)((2-NITROPHENYL)SULFONYL)AMINE 1-((4-(3-CHLORO-5-(TRIFLUOROMETHYL)(2-PYRIDYL))PIPERAZINYL)SULFONYL)-2-NITROBENZENE 2-NITRO-1-((4-(5-(TRIFLUOROMETHYL)(2-PYRIDYL))PIPERAZINYL)SULFONYL)BENZENE 2,3-DIHYDRO-N,N-DIMETHYL-7-(1H)-INDOLESULPHONAMIDE 2-AMINO-N-QUINOLIN-8-YL-BENZENESULFONAMIDE 1-[(ETHYLAMINO)CARBONYL]-7-(DIMETHYLAMINOSULPHONYL)-2,3-DIHYDRO-(1H)-INDOLE

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