2-Amino-4-trifluoromethyl-benzoic acid methyl ester

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2-Amino-4-trifluoromethyl-benzoic acid methyl ester Basic information
Product Name:2-Amino-4-trifluoromethyl-benzoic acid methyl ester
Synonyms:2-amino-4-(trifluoromethyl)benzoate;Methyl 2-aMino-3-chloro-5-trifluoroMethoxybenzoate;Benzoic acid, 2-aMino-4-(trifluoroMethyl)-, Methyl ester;2-Amino-4-trifluoromethyl-benzoic acid methyl ester 97%;Methyl 2-amino-4-(trifluoromethyl)benzoate;2-Amino-4-trifluoromethyl-benzoic acid methyl ester
CAS:61500-87-6
MF:C9H8F3NO2
MW:219.16
EINECS:
Product Categories:Fluorine series;Aromatic Esters;Aromatic Building Blocks
Mol File:61500-87-6.mol
2-Amino-4-trifluoromethyl-benzoic acid methyl ester Structure
2-Amino-4-trifluoromethyl-benzoic acid methyl ester Chemical Properties
Melting point 65-68 °C(Solv: ethanol (64-17-5); water (7732-18-5))
Boiling point 267.5±40.0 °C(Predicted)
density 1.343±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in Methanol
form powder to crystal
pka1.06±0.10(Predicted)
color White to Light yellow to Light orange
InChIInChI=1S/C9H8F3NO2/c1-15-8(14)6-3-2-5(4-7(6)13)9(10,11)12/h2-4H,13H2,1H3
InChIKeyDZICUHOFOOPVFM-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=C(C(F)(F)F)C=C1N
Safety Information
HS Code 2922498590
MSDS Information
2-Amino-4-trifluoromethyl-benzoic acid methyl ester Usage And Synthesis
Uses2-Amino-4-trifluoromethylbenzoic Acid Methyl Ester is an intermediate used to prepare quinazolinedione sulfonamides as competitive AMPA receptor antagonists. It is also used in the synthesis of (arylamino)pyrimidobenzazepinones and pyrimidobenzazepinethiones as inhibitors of polo-like kinase 1 and potential antitumor agents.
Synthesis
Methyl 2-nitro-4-(trifluoromethyl)benzoate

228418-45-9

2-AMINO-4-TRIFLUOROMETHYL-BENZOIC ACID METHYL ESTER

61500-87-6

Step 2; Preparation of methyl 2-amino-4-trifluoromethylbenzoate; Methyl 2-nitro-4-(trifluoromethyl)benzoate (106 g, 425 mmol) was dissolved in ethanol. To a slurry of 10% palladium carbon (11.0 g) in ethyl acetate (200 mL) was added ethyl acetate (2.2 L), and the suspension was stirred for 3 h at room temperature and 60 °C under a hydrogen atmosphere. Upon completion of the reaction, the suspension was filtered through a Celite pad and the pad was washed with additional ethyl acetate. The filtrate was concentrated under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography using isohexane/ethyl acetate (9:1) as eluent to afford methyl 2-amino-4-trifluoromethylbenzoate as a white crystalline solid (84 g, 95% yield).

References[1] Patent: WO2006/2342, 2006, A1. Location in patent: Page/Page column 55-56
[2] Patent: US2004/102636, 2004, A1
[3] Patent: US2008/269265, 2008, A1. Location in patent: Page/Page column 10
[4] Patent: EP1449834, 2004, A2. Location in patent: Page 16
[5] Patent: EP1042305, 2005, B1. Location in patent: Page/Page column 21
2-Amino-4-trifluoromethyl-benzoic acid methyl ester Preparation Products And Raw materials
Raw materialsMethyl 2-nitro-4-(trifluoromethyl)benzoate-->Methanol-->Methyl, azo--->2-Amino-4-(trifluoromethyl)benzoic acid-->Ethyl acetate-->Hydrogen
Tag:2-Amino-4-trifluoromethyl-benzoic acid methyl ester(61500-87-6) Related Product Information
Tosyl chloride 2-Nitro-4-trifluoromethylbenzoic acid 2-[(3-Carboxyphenyl)methylamino]-4-trifluoromethyl-benzoic acid t-butyl ester Ethyl 2-amino-4-trifluoromethylbenzoate 2-Amino-4-trifluoromethyl-benzoic acid t-butyl ester 2-Amino-4-trifluoromethyl-benzoic acid methyl ester 2-Amino-4-(trifluoromethyl)benzoic acid