Identification | Back Directory | [Name]
Methyl 3-amino-4-(methylamino)benzenecarboxylate | [CAS]
66315-16-0 | [Synonyms]
Methyl 3-aMino-4-(MethylaMino)benzoate 3-Amino-4-(methylamino)benzoesaeure-methylester 3-Amino-4-methylamino-benzoic acid methyl ester Methyl 3-amino-4-(methylamino)benzenecarboxylate Benzoic acid, 3-amino-4-(methylamino)-, methyl ester | [Molecular Formula]
C9H12N2O2 | [MDL Number]
MFCD12922710 | [MOL File]
66315-16-0.mol | [Molecular Weight]
180.2 |
Chemical Properties | Back Directory | [Melting point ]
103-105° | [Boiling point ]
346.5±32.0 °C(Predicted) | [density ]
1.208±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [pka]
5.40±0.11(Predicted) | [Appearance]
Gray to dark gray Solid |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of methyl 3-amino-4-(methylamino)benzoate from methyl 4-(methylamino)-3-nitrobenzoate: Methyl 4-(methylamino)-3-nitrobenzoate (540 mg, 2.5 mmol) was dissolved in a solvent mixture of ethyl acetate and methanol (2:1 v/v/v, 20 mL). A 10% palladium-carbon catalyst (5 mol%) was added to the solution under nitrogen protection. The reaction mixture was placed in a hydrogen atmosphere and the reaction was stirred for 4 hours. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration. The filtrate was concentrated under reduced pressure to afford the target product methyl 3-amino-4-(methylamino)benzoate. The product was characterized by LC-MS with molecular ion peak [M + 1] = 181.1. yield: 441 mg (100% yield). | [References]
[1] Patent: EP1502916, 2005, A1. Location in patent: Page 440 [2] Patent: WO2007/69053, 2007, A1. Location in patent: Page/Page column 34 [3] Patent: WO2008/65508, 2008, A1. Location in patent: Page/Page column 32-33; 38-40 [4] Patent: WO2017/147102, 2017, A1. Location in patent: Paragraph 00126-00127 [5] Patent: WO2017/100594, 2017, A1. Location in patent: Paragraph 00132 |
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