ChemicalBook--->CAS DataBase List--->464913-11-9

464913-11-9

464913-11-9 Structure

464913-11-9 Structure
IdentificationBack Directory
[Name]

3-AMINO-2-HYDROXY-N,N-DIMETHYLBENZAMIDE
[CAS]

464913-11-9
[Synonyms]

3-aMino-N,N-diMethylsalicylaMide
3-AMINO-2-HYDROXY-N,N-DIMETHYLBENZAMIDE
Benzamide, 3-amino-2-hydroxy-N,N-dimethyl-
[Molecular Formula]

C9H12N2O2
[MDL Number]

MFCD13191893
[MOL File]

464913-11-9.mol
[Molecular Weight]

180.2
Chemical PropertiesBack Directory
[Boiling point ]

374.5±37.0 °C(Predicted)
[density ]

1.239±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

8.07±0.35(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Hazard InformationBack Directory
[Uses]

3-Amino-2-hydroxy-N,N-dimethylbenzamide is a useful research chemical compound used int he synthesis of 3,4-diaminocyclobut-3-ene-1,2-dione CXCR2 antagonists.
[Synthesis]

2-hydroxy-N,N-diMethyl-3-nitrobenzaMide

66952-65-6

3-AMINO-2-HYDROXY-N,N-DIMETHYLBENZAMIDE

464913-11-9

Step 7 Synthesis of 3-amino-2-hydroxy-N,N-dimethylbenzamide: 33.5 g of 2-hydroxy-N,N-dimethyl-3-nitrobenzamide was dissolved in 600 mL of ethanol to form a solution. To this solution was added 3.35 g of Pd/C catalyst (suspended in 10 mL of 70 mL of ethanol). The reaction mixture was placed under 2 bar hydrogen atmosphere and the reaction was stirred overnight. The progress of the reaction was monitored by thin layer chromatography (TLC) and high performance liquid chromatography (HPLC) (HPLC retention time t = 0.66 min, molecular ion peak M + 181). Upon completion of the reaction, the reaction mixture was filtered through a diatomaceous earth pad to remove the catalyst. The filtrate was concentrated under reduced pressure to give 29 g of brown oily solid, 3-amino-2-hydroxy-N,N-dimethylbenzamide, in 100% yield.

[References]

[1] Patent: US2014/296254, 2014, A1. Location in patent: Paragraph 0102
[2] Patent: US2014/309208, 2014, A1. Location in patent: Paragraph 0110; 0115
[3] Patent: US2015/87675, 2015, A1. Location in patent: Paragraph 0152
[4] Patent: WO2004/33440, 2004, A1. Location in patent: Page 166
[5] Patent: US2004/147559, 2004, A1. Location in patent: Page 80
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